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    Tanvex BioPharma Completes Acquisition of Bora Biologics

    20 Jan 2025

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    Bora Biologics, DotBio Enter Strategic CMC Development Collab

    09 Jan 2025

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    Bora to Expand Rare Disease Portfolio with Acquisition of Pyros

    26 Oct 2024

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    Bora Pharmaceuticals is a premier global contract development and manufacturing organization (CDMO), specializing in formulation development, clinical and commercial manufacturing and packaging of complex oral solid dose, liquid, and semi-solid pharmaceutical products for clinical and commercial uses.
    From cell-line development and formulation to analytical services and clinical cGMP manufacturing, Bora now provides tailored development and manufacturing services to biologics developers. Bora operates nine cGMP manufacturing sites in Asia, Canada, and the United States, and delivers to over 100 markets worldwide.

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    6F, No 69, Xing'ai Road, Neihu District, Taipei City 114
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    +1 844636-BORA (2672) // +1 616636-BORA (2672)
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    marketing@bora-corp.com
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    https://www.boracdmo.com
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    North America facility:
    Bora Pharmaceuticals – North America

    Taiwan facilities:
    Bora Pharmaceuticals – Taoyuan
    Bora Pharmaceuticals – Tainan
    Bora Pharmaceuticals – Zhongli
    Bora Pharmaceuticals – Zhunan
    Bora Biologics – Zhubei

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    Ophthalmics

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    Facilities in Taiwan

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    Cell Line Development

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    Outstanding Company of the Year Award at Bio-Asia Taiwan 2023

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    Biologics CDMO

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    Small Molecule CDMO

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    Bora new CMO for Commercial Manufacturing of Phexxi® for Evofem

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    Extrusion-Spheronization for Controlled Release Forms

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    CDMO Activity Tracker: Bora, PolPharma make acquisitions; Evonik, EUROAPI, Porton announce technological expansions

    CDMO Activity Tracker: Bora, PolPharma make acquisitions; Evonik, EUROAPI, Porton announce technological expansions

    The contract development and manufacturing organization (CDMO) space continued to grow at an impressive pace in the second half (H2) of 2024, with significant progress being made across cell and gene therapies (CGTs), antibody-drug conjugates (ADCs), novel drug modalities, and digital solutions.Some of the key players in the CDMO space include Lonza, EUROAPI, Evonik, SEQENS, Fujifilm Diosynth Biotechnologies, Quotient Sciences, Axplora, PolPharma, and Famar from Europe; Mission CDMO, LGM Pharma, Veranova, and Thermo Fisher from the US; and Samsung Biologics, Bora Pharmaceuticals, and Porton Pharma Solutions from Asia. Texas-based Mission CDMO has been in the pharma industry for over 75 years. Today, it is known for its comprehensive contract services and high-quality manufacturing capabilities that have reinforced its position as a trusted partner. View CDMO Activity Tracker for H2 2024 (Free Excel Available)Bora, PolPharma drive CDMO acquisitions; Samsung Biologics clocks over US$ 4 bn in contract valueThe second half of 2024 saw several high-value acquisitions and expansions that reshaped the CDMO landscape. South Korea-based Samsung Biologics clocked a cumulative contract value of over US$ 4 billion. It signed its largest manufacturing deal with an Asia-based pharmaceutical company, valued at US$ 1.24 billion. It also announced a series of manufacturing deals with a European drugmaker worth over US$ 668 million. Samsung Biologics is also building a dedicated ADC facility that is likely to be complete soon. Taiwan’s largest CDMO, Bora Pharmaceuticals, announced its second acquisition of the year. It bought New Jersey-based Pyros Pharmaceuticals, a developer of rare disease treatments. Pyros recently launched Vigafyde, the only ready-to-use vigabatrin oral solution and the first new product approved to treat infantile spasms in 15 years. Bora also announced a strategic investment in Tanvex Biopharma, thereby creating a global platform for biologics development and supply.PolPharma acquired Ziołolek, a renowned manufacturer of dermatological products, medical devices, and OTC medicines, thereby expanding its product portfolio. It also launched a state-of-the-art HPAPI (highly potent active pharmaceutical ingredients) facility in Poland, which is being seen as another step towards securing Europe’s drug supply chain.In other developments, Avid Bioservices got acquired by funds managed by Ampersand and British healthcare investment firm GHO Capital Partners in an all-cash deal worth US$ 1.1 billion. And Agilent Technologies agreed to acquire Canadian specialty CDMO Biovectra for US$ 925 million, thereby enhancing its capabilities in gene-editing technologies and sterile fill-finish services. View CDMO Activity Tracker for H2 2024 (Free Excel Available) Evonik, EUROAPI, Porton Pharma, GSK announce tieups, technological expansionsSeveral CDMOs announced new collaborations and acquired new capabilities to enhance their service offerings. Evonik expanded its formulation capabilities for lipid nanoparticles used for mRNA and gene therapies through a collaboration with KNAUER Wissenschaftliche Geräte. This partnership aims to expand Evonik’s portfolio of biosolutions.Evonik is also restructuring its keto and pharma amino acid business to focus on strategic core growth areas. Evonik launched Eudracap colon functional capsules for targeted delivery of oral drugs. These ready-to-fill capsules are designed to release their contents specifically in the colon, improving the efficacy of treatments for various gastrointestinal conditions. Evonik also opened a new facility for drying aqueous dispersions of Eudragit polymers in Darmstadt, Germany. This facility will enhance Evonik’s capabilities in producing high-quality polymers for pharmaceutical applications.EUROAPI launched a new AI-powered Electronic Batch Record solution in collaboration with Aizon to enhance manufacturing productivity. This collaboration aims to digitize operations towards more data-driven manufacturing, focusing on small-scale productions and highly flexible plants.Porton Pharma Solutions has expanded its reach through several strategic initiatives. In October, Porton entered into a partnership with Shanghai InnoStar to enhance its service offerings beyond small molecules, targeting peptides, oligonucleotide drugs, conjugated drugs, and advanced therapies. It continued to grow its capabilities by enhancing its GMP manufacturing capacity in Fengxian, Shanghai (China). The facility’s expansion is aimed at increasing the production of novel therapies, including peptides and oligonucleotide drugs. These moves are part of Porton’s broader strategy to position itself at the forefront of advanced pharmaceutical manufacturing.Corden Pharma is investing € 900 million (US$ 985 million) over the next three years to expand its peptide platform facilities in Colorado (US) and Europe. While the US site will help meet the rising demand for GLP-1 peptides, in Europe, CordenPharma will construct a greenfield facility for small to large-scale peptide development and manufacturing.CDMO Touchlight signed a licensing agreement with GSK that grants the drug behemoth non-exclusive rights to use Touchlight’s proprietary enzymatic doggybone DNA (dbDNA) technology for the development and production of mRNA-based products, particularly vaccines. Curia also integrated enzymatic dbDNA solutions through a collaboration with Touchlight, enhancing mRNA production for vaccine and cancer therapies. View CDMO Activity Tracker for H2 2024 (Free Excel Available) Lonza, Merck, Dr. Reddy’s owned Aurigene invest in cell and gene therapiesThe CGT space continued to draw both deals and investments. Lonza and Vertex signed a long-term commercial supply agreement for Casgevy, the world’s first CRISPR/Cas9 gene-edited cell therapy, to treat sickle cell disease and beta thalassemia. This agreement includes manufacturing at Lonza’s Geleen (the Netherlands) cell therapy manufacturing facility, with plans to expand to Portsmouth, New Hampshire (US).Miltenyi Biotec began manufacturing lentiviral vectors for Adaptimmune’s Tecelra, the first engineered TCR T-cell therapy for the rare soft tissue cancer synovial sarcoma approved by the US Food and Drug Administration.Merck KGaA commenced commercial production at its first GMP-compliant manufacturing line for cell culture media (CCM) in China. This facility addresses the growing local demand for quality custom CCM used in biopharmaceuticals, vaccines, and novel therapeutics.Aurigene and Edity Therapeutics announced a strategic collaboration in cell therapy, with Aurigene providing cell therapy discovery services to support Edity’s clinical development. Additionally, Aurigene and its parent, Dr. Reddy’s Laboratories, signed a memorandum of understanding (MoU) with Kainomyx for the development and commercialization of an affordable anti-malarial drug. ProBio and UCI Therapeutics signed an MoU for a comprehensive collaboration in gene delivery technologies, including viral and non-viral approaches. Additionally, Korea’s VaxCell-Bio partnered with ProBio to accelerate the development of its chimeric antigen receptor (CAR)-related therapies.The ADC market continued to be a hotbed of innovation and strategic expansion. Merck KGaA invested € 70 million (US$ 75 million) to triple its ADC manufacturing capacity at its Missouri (US) facility, aiming to support the rising demand for oncology therapies.Sterling Pharma entered into a partnership with GlycoNex to support the clinical trials of their ADCs that target solid tumors. And, NJ Bio and Charles River Laboratories also announced a collaboration to optimize ADC manufacturing.The adeno-associated viral (AAV) vector field also saw activity with Rentschler Biopharma and Forge Biologics announcing the launch of a new service offering and a manufacturing platform, respectively. Similarly, Andelyn Biosciences was selected by Hubble Therapeutics to manufacture clinical grade AAV.Meanwhile, Lonza has gone in for a restructuring exercise in order to become a “pure-play CDMO”. It has exited its capsules and health ingredients business, and adopted a new organizational structure. The Swiss CDMO has also extended a collaboration with a major global biopharmaceutical partner for commercial-scale manufacture of ADCs. View CDMO Activity Tracker for H2 2024 (Free Excel Available) Our viewAs pharmaceutical development becomes increasingly complex, CDMOs are no longer just manufacturing partners, but critical innovation hubs. Little wonder then that 2024’s biggest pharma deal was in the CDMO space – Novo Holdings’ US$ 16.5 billion buyout of Catalent. This trend should gather momentum. We expect more M&A activity in this space in 2025. 
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    19 Dec 2024
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    CDMO Activity Tracker: Novo’s parent buys Catalent for US$ 16.5 bn; Fujifilm, Merck KGaA, Axplora expand capabilities

    CDMO Activity Tracker: Novo’s parent buys Catalent for US$ 16.5 bn; Fujifilm, Merck KGaA, Axplora expand capabilities

    During the first half (H1) of 2024, the global contract development and manufacturing organization (CDMO) landscape was driven by the escalating demand for complex drug development and manufacturing.With the industry grappling with constantly evolving therapeutic modalities, CDMOs are racing to invest in cutting-edge technologies and infrastructure to meet the growing needs of pharmaceutical and biotech companies.Some of the key players in the CDMO space are Catalent, EUROAPI, Lonza, Axplora, Thermo Fisher, SEQENS, Samsung Biologics, Fujifilm Diosynth Biotechnologies, Quotient Sciences, Famar, LGM Pharma, Veranova, and Evonik. View CDMO Activity Tracker for H1 2024 (Free Excel Available)Novo’s parent buys Catalent for US$ 16.5 bn; Bora, Lonza, Siegfried expand US footprintDuring H1 2024, several European and Asian drugmakers expanded their footprints in the US. In February, Novo Nordisk’s parent company, the Novo Nordisk Foundation, announced the acquisition of Catalent through its investment arm Novo Holdings for US$ 16.5 billion. Novo Holdings plans to sell three of Catalent’s “fill-finish” sites to Novo Nordisk for US$ 11 billion. The deal is expected to allow the Danish drugmaker “to serve significantly more people living with diabetes and obesity,” a company statement said.Taiwan-headquartered Bora Pharmaceuticals forged ahead with its expansion plans in the US market by acquiring Minnesota-based generics manufacturer Upsher-Smith Laboratories. Emergent BioSolutions said it is selling its Maryland facility to an affiliate of Bora. This site in Camden is part of its CDMO, Emergent Bioservices, and offers clinical and commercial non-viral aseptic fill/finish services on four fill lines, including lyophilization, formulation development, and support services.Swiss drugmaker Lonza has agreed to acquire Genentech’s manufacturing facility in California, US, from Roche for US$ 1.2 billion in cash. The site, located in the city of Vacaville, is one of the largest biologics manufacturing facilities in the world by volume.Lonza also launched an artificial intelligence-driven route design technology for choosing the optimal synthetic pathway to manufacture novel APIs.Switzerland’s Siegfried is acquiring a Wisconsin (US)-based CDMO that specializes in early-phase development and manufacturing services from Curia Global to strengthen its capabilities in North America. Siegfried will further develop the site into its North American Siegfried Acceleration Hub for early-phase CDMO services. View CDMO Activity Tracker for H1 2024 (Free Excel Available) Merck Millipore, SK Bioscience lead CGT boom; Fujifilm, Axplora, expand CDMO capabilitiesThe burgeoning field of cell and gene therapies (CGTs) is driving significant investments in CDMOs. CGTs saw considerable deal-making too. Merck KGaA agreed to buy Wisconsin-based Mirus Bio for US$ 600 million. Mirus Bio is a specialist in the development and commercialization of transfection reagents that are used to help introduce genetic material into cells. These reagents play a key role in the production of viral vectors for CGTs.Similarly, South Korea’s SK Bioscience acquired a 60 percent stake in IDT Biologika GmbH for KRW 339 billion (US$ 244 million). IDT Biologika is a 104-year-old German company that ranks among the top 10 vaccine producers in the world.CDMOs are also expanding their capabilities in order to lead innovation for their pharmaceutical partners. Fujifilm Diosynth Biotechnologies is investing US$ 1.2 billion in its large-scale cell culture CDMO business to further expand its end-to-end bio-manufacturing facility in North Carolina, bringing the total investment in the facility to over US$ 3.2 billion. Similarly, Merck KGaA owned MilliporeSigma made its biggest investment in the Asia-Pacific region in March when it invested € 300 million (US$ 327 million) in a new bioprocessing production center in Daejeon, South Korea.German CDMO giant Axplora is investing € 8 million (US$ 8.73 million) to expand capacity for antibody drug conjugate (ADC) payload manufacturing at its Le Mans site in France. Catalent completed upgrades to its capsule filling capabilities of dry powders for inhalation to handle potent drugs at its Boston facility. This now positions Catalent as the CDMO with the largest GMP capacity for capsule spray-dried and carrier-based inhaled powders.LGM Pharma increased its Analytical Testing Services (ATS) by 50 percent with a US$ 2 million investment and introduced new suppository manufacturing capabilities to its CDMO portfolio. Minakem has invested in a new production unit in Montreal, Canada, for steroid APIs. View CDMO Activity Tracker for H1 2024 (Free Excel Available) EUROAPI kicks off four-year sweeping plan; LegoChem partners Samsung Biologics for ADC programSanofi’s spinoff EUROAPI marked 2024 as a “transition year”, setting in motion its Focus-27 plan for profitable growth in the future. The sweeping four-year plan includes a streamlined value-added portfolio focused on highly differentiated and profitable APIs, and a CDMO focused on late-stage and high-value complex small molecules and tides supported by unique technological platforms. The leading French small molecules player signed a five-year collaboration with Ireland’s Priothera wherein EUROAPI will develop and industrialize the manufacturing process of an innovative, complex molecule for blood cancers – mocravimod. The project will be carried out at EUROAPI’s site in Budapest, which is its center of excellence for complex chemistry.South Korea’s CDMO powerhouse Samsung Biologics has partnered LegoChem Biosciences and will provide antibody development and drug substance manufacturing services as a part of LegoChem’s ADC program designed to treat solid tumors. LegoChem aims to submit an investigational new drug application to the US Food and Drug Administration (FDA) in the first half of 2025. Aurigene and Vipergen have joined forces to offer DNA-encoded library (DEL) screening for drug discovery. By combining Aurigene’s drug discovery capabilities with Vipergen’s DEL screening technologies, they seek to create a powerful tool that can quickly test over a billion small-molecule compounds against different disease targets. Dr. Reddy’s Laboratories’ company Aurigene also inaugurated its biologics facility spread across 70,000 square feet.Chinese biotech startup Pleryon is collaborating with France’s SEQENS, a leader in specialty ingredients, to develop and manufacture the former’s lead candidate, an innovative polymer to treat osteoarthritis. Famar is collaborating with Lavipharm and will serve as the contract manufacturer for the latter’s recently added analgesic pharmaceutical products — Lonarid N and Lonalgal. View CDMO Activity Tracker for H1 2024 (Free Excel Available) Our view Key trends observed in H1 2024 include a surge in investments for fill-finish facilities, a growing emphasis on cell and gene therapies, and advancements in ADC manufacturing. With the proliferation of these new classes of drugs, the CDMO space has been rapidly changing in recent years. In the future, the integration of digital technologies, such as AI and automation, will be a key differentiator for CDMOs looking to optimize their operations and accelerate drug development timelines. 
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    Tanvex BioPharma Completes Acquisition of Bora Biologics
    Tanvex BioPharma Completes Acquisition of Bora Biologics

    20 Jan 2025

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    https://bora-corp.com/tanvex-acquisition-bora-biologics/

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    20 Jan 2025
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    Bora Biologics, DotBio Enter Strategic CMC Development Collab
    Bora Biologics, DotBio Enter Strategic CMC Development Collab

    09 Jan 2025

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    https://bora-corp.com/bora-biologics-announces-strategic-collaboration-to-accelerate-key-cmc-development-of-dotbios-tri-specific-antibody-to-treat-cancer/

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    09 Jan 2025
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    Bora to Expand Rare Disease Portfolio with Acquisition of Pyros
    Bora to Expand Rare Disease Portfolio with Acquisition of Pyros

    26 Oct 2024

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    https://bora-corp.com/bora-pharmaceuticals-to-expand-rare-disease-portfolio-with-acquisition-of-us-based-pyros-pharmaceuticals/

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    26 Oct 2024
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    Bora Pharmaceuticals Appoints Division President of CDMO Business
    Bora Pharmaceuticals Appoints Division President of CDMO Business

    04 Oct 2024

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    https://bora-corp.com/bora-appoints-j-d-mowery-as-first-division-president-of-its-cdmo-business/

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    04 Oct 2024
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    Formosa Ships APP13007 To US For Commercialization
    Formosa Ships APP13007 To US For Commercialization

    09 Sep 2024

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    https://www.prnewswire.com/news-releases/formosa-pharmaceuticals-makes-first-shipment-of-app13007-clobetasol-propionate-ophthalmic-suspension-0-05-to-the-united-states-for-commercialization-302241470.html

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    09 Sep 2024
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    Tanvex Appoints Biopharma Industry Veteran Stephen Lam as CEO
    Tanvex Appoints Biopharma Industry Veteran Stephen Lam as CEO

    05 Sep 2024

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    https://bora-corp.com/tanvex-appoints-biopharma-industry-veteran-stephen-lam-as-ceo/

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    05 Sep 2024
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    Drugs in Development

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    Bora Biologics, DotBio Enter Strategic CMC Development Collaboration

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    The collaboration aims to advance the development of DotBio’s Tri-Specific Antibody DB007 for the treatment of Cancer.


    Lead Product(s): DB007

    Therapeutic Area: Oncology Brand Name: DB007

    Study Phase: PreclinicalProduct Type: Antibody

    Sponsor: DotBio

    Deal Size: Undisclosed Upfront Cash: Undisclosed

    Deal Type: Collaboration January 09, 2025

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    Bora Pharmaceuticals

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    Lead Product(s) : DB007

    Therapeutic Area : Oncology

    Highest Development Status : Preclinical

    Partner/Sponsor/Collaborator : DotBio

    Deal Size : Undisclosed

    Deal Type : Collaboration

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    Bora Biologics, DotBio Enter Strategic CMC Development Collaboration

    Details : The collaboration aims to advance the development of DotBio’s Tri-Specific Antibody DB007 for the treatment of Cancer.

    Product Name : DB007

    Product Type : Antibody

    Upfront Cash : Undisclosed

    January 09, 2025

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    Bora and Celltrion Join Forces To Distribute Oral Drugs Across APAC

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    Under the partnership, Bora will manufacture and commercialize a range of oral dosage form drugs (OSD), including CT-G20, a hypertrophic cardiomyopathy treatment candidate, across the APAC region.


    Lead Product(s): CT-G20

    Therapeutic Area: Cardiology/Vascular Diseases Brand Name: CT-G20

    Study Phase: Phase IProduct Type: Other Small Molecule

    Sponsor: Celltrion

    Deal Size: Undisclosed Upfront Cash: Undisclosed

    Deal Type: Partnership June 04, 2023

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    Bora Pharmaceuticals

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    Lead Product(s) : CT-G20

    Therapeutic Area : Cardiology/Vascular Diseases

    Highest Development Status : Phase I

    Partner/Sponsor/Collaborator : Celltrion

    Deal Size : Undisclosed

    Deal Type : Partnership

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    Bora and Celltrion Join Forces To Distribute Oral Drugs Across APAC

    Details : Under the partnership, Bora will manufacture and commercialize a range of oral dosage form drugs (OSD), including CT-G20, a hypertrophic cardiomyopathy treatment candidate, across the APAC region.

    Product Name : CT-G20

    Product Type : Other Small Molecule

    Upfront Cash : Undisclosed

    June 04, 2023

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    Bora Pharmaceuticals Partners with TaiRx

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    CVM-1118 (foslinanib) is a new small molecule chemical entity and a potential anti-cancer agent in numerous human cancer cell lines with strong anti-cancer activity, high safety margin, and multiple mechanisms of actions in targeting cancer-specific factors.


    Lead Product(s): Foslinanib,Sorafenib

    Therapeutic Area: Oncology Brand Name: CVM-1118

    Study Phase: Phase IIProduct Type: Other Small Molecule

    Sponsor: TaiRx

    Deal Size: Undisclosed Upfront Cash: Undisclosed

    Deal Type: Partnership September 27, 2022

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    Bora Pharmaceuticals

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    Lead Product(s) : Foslinanib,Sorafenib

    Therapeutic Area : Oncology

    Highest Development Status : Phase II

    Partner/Sponsor/Collaborator : TaiRx

    Deal Size : Undisclosed

    Deal Type : Partnership

    DEALS_DEV arrow-down

    Bora Pharmaceuticals Partners with TaiRx

    Details : CVM-1118 (foslinanib) is a new small molecule chemical entity and a potential anti-cancer agent in numerous human cancer cell lines with strong anti-cancer activity, high safety margin, and multiple mechanisms of actions in targeting cancer-specific fact...

    Product Name : CVM-1118

    Product Type : Other Small Molecule

    Upfront Cash : Undisclosed

    September 27, 2022

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    API & Drug Product Development

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    Formulation Development

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    LIQUID FORMULATION DEVELOPMENT S...

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    Pharma Service : API & Drug Product Development

    Bora Pharmaceuticals

    Bora is a contract development and manufacturing organization (CDMO) that offers formulation development of liquid dosage forms, such as solution, syrup, and suspension, with small-scale (10L to 600L) capacities and semi-manual small-scale bottle filling.

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    Category : Formulation Development

    Sub Category : Liquid Formulation

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    Pharma Service : API & Drug Product Development

    LIQUID FORMULATION DEVELOPMENT SERVICES

    Bora is a contract development and manufacturing organization (CDMO) that offers formulation development of liquid dosage forms, such as solution, syrup, and suspension, with small-scale (10L to 600L) capacities and semi-manual small-scale bottle filling.

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    CDMO FOR TABLETS

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    Pharma Service : API & Drug Product Development

    Bora Pharmaceuticals

    Bora CDMO offers development for enteric-coated, matrix, bi-layered, and miniature tablets. Its formulation development teams have experience supporting commercial development and manufacturing strategies across a wide range of drug programs.

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    Category : Formulation Development

    Sub Category : Tablet

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    Pharma Service : API & Drug Product Development

    CDMO FOR TABLETS

    Bora CDMO offers development for enteric-coated, matrix, bi-layered, and miniature tablets. Its formulation development teams have experience supporting commercial development and manufacturing strategies across a wide range of drug programs.

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    CDMO for Tablets

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    Market
    Place

    03

    FORMULATION DEVELOPMENT OF CAPSU...

    Taiwan
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    Virtual BoothBora Pharmaceuticals- Making success more certain.

    Pharma Service : API & Drug Product Development

    Bora Pharmaceuticals

    Bora CDMO offers formulation development of capsules, single & combination fills, including powders, pellets, tablets and micro-tablets. It supports commercial formulation development & manufacturing strategies across a wide range of drug programs.

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    Category : Formulation Development

    Sub Category : Capsule

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    • EDQM
    • WHO-GMP

    Virtual BoothBora Pharmaceuticals- Making success more certain.

    Pharma Service : API & Drug Product Development

    FORMULATION DEVELOPMENT OF CAPSULES

    Bora CDMO offers formulation development of capsules, single & combination fills, including powders, pellets, tablets and micro-tablets. It supports commercial formulation development & manufacturing strategies across a wide range of drug programs.

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    Formulation Development of Capsules

    Service
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    Capabilities
    #ServicesBio

    Market
    Place

    04

    TOPICAL FORMULATION DEVELOPMENT

    Taiwan
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    Virtual BoothBora Pharmaceuticals- Making success more certain.

    Pharma Service : API & Drug Product Development

    Bora Pharmaceuticals

    Bora is a contract development and manufacturing organization (CDMO) that specializes in the formulation development, commercial manufacturing, and packaging of topical drug products such as creams, ointments, and gels for clinical and commercial uses.

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    Category : Formulation Development

    Sub Category : Topical

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    Virtual BoothBora Pharmaceuticals- Making success more certain.

    Pharma Service : API & Drug Product Development

    TOPICAL FORMULATION DEVELOPMENT

    Bora is a contract development and manufacturing organization (CDMO) that specializes in the formulation development, commercial manufacturing, and packaging of topical drug products such as creams, ointments, and gels for clinical and commercial uses.

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    Topical Formulation Development

    Service
    Web Link

    Capabilities
    #ServicesBio

    Market
    Place

    05

    CDMO FOR OPHTHALMIC FORMULATIONS

    Taiwan
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    Virtual BoothBora Pharmaceuticals- Making success more certain.

    Pharma Service : API & Drug Product Development

    Bora Pharmaceuticals

    Bora’s Taoyuan facility, the first FDA-approved ophthalmic site in Taiwan, further strengthens Bora’s position as a global CDMO leader. It can produce all the ophthalmic forms, such as, multi-dose with and without preservatives, gels, creams & ointments.

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    Category : Formulation Development

    Sub Category : Ophthalmic

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    Virtual BoothBora Pharmaceuticals- Making success more certain.

    Pharma Service : API & Drug Product Development

    CDMO FOR OPHTHALMIC FORMULATIONS

    Bora’s Taoyuan facility, the first FDA-approved ophthalmic site in Taiwan, further strengthens Bora’s position as a global CDMO leader. It can produce all the ophthalmic forms, such as, multi-dose with and without preservatives, gels, creams & ointments.

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    CDMO for Ophthalmic Formulations

    Service
    Web Link

    Capabilities
    #ServicesBio

    Market
    Place

    06

    FORMULATION DEVELOPMENT & CLINIC...

    Taiwan
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    Virtual BoothBora Pharmaceuticals- Making success more certain.

    Pharma Service : API & Drug Product Development

    Bora Pharmaceuticals

    Bora is a premier international CDMO specializing in formulation development, clinical & commercial manufacturing & packaging of complex oral solid-dose, liquid & semi-solid pharmaceutical products for clinical & commercial uses.

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    Category : Formulation Development

    Sub Category : Clinical Supply

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    • WHO-GMP

    Virtual BoothBora Pharmaceuticals- Making success more certain.

    Pharma Service : API & Drug Product Development

    FORMULATION DEVELOPMENT & CLINICAL SUPPLY

    Bora is a premier international CDMO specializing in formulation development, clinical & commercial manufacturing & packaging of complex oral solid-dose, liquid & semi-solid pharmaceutical products for clinical & commercial uses.

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    Formulation Development & Clinical Supply

    Service
    Web Link

    Capabilities
    #ServicesBio

    Market
    Place

    07

    DEVELOPMENT OF SEMI-SOLID DOSAGE...

    Taiwan
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    German Wound Congress
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    Virtual BoothBora Pharmaceuticals- Making success more certain.

    Pharma Service : API & Drug Product Development

    Bora Pharmaceuticals

    Bora is a premier international CDMO specializing in formulation development, commercial manufacturing, and packaging of semi-solid topical products such as creams, gels, and ointments for clinical and commercial uses.

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    Category : Formulation Development

    Sub Category : Cream / Gel / Lotion / Ointment

    • fda
    • EDQM
    • WHO-GMP

    Virtual BoothBora Pharmaceuticals- Making success more certain.

    Pharma Service : API & Drug Product Development

    DEVELOPMENT OF SEMI-SOLID DOSAGE FORMS

    Bora is a premier international CDMO specializing in formulation development, commercial manufacturing, and packaging of semi-solid topical products such as creams, gels, and ointments for clinical and commercial uses.

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    Development of Semi-solid Dosage Forms

    Service
    Web Link

    Capabilities
    #ServicesBio

    Market
    Place

    08

    CDMO FOR NASAL SPRAYS

    Taiwan
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    German Wound Congress
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    • fda
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    Virtual BoothBora Pharmaceuticals- Making success more certain.

    Pharma Service : API & Drug Product Development

    Bora Pharmaceuticals

    Bora is a premier international CDMO specializing in formulation development, manufacturing & packaging of nasal formulations and liquid pharmaceuticals. It has a dedicated manufacturing area and a high-speed line for nasal sprays.

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    Category : Formulation Development

    Sub Category : Inhalation / Nasal

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    • EDQM
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    Virtual BoothBora Pharmaceuticals- Making success more certain.

    Pharma Service : API & Drug Product Development

    CDMO FOR NASAL SPRAYS

    Bora is a premier international CDMO specializing in formulation development, manufacturing & packaging of nasal formulations and liquid pharmaceuticals. It has a dedicated manufacturing area and a high-speed line for nasal sprays.

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    CDMO for Nasal Sprays

    Service
    Web Link

    Capabilities
    #ServicesBio

    Market
    Place

    09

    FORMULATION SCALE UP CAPABILITIE...

    Taiwan
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    German Wound Congress
    Not Confirmed
    • fda
    • EDQM
    • WHO-GMP

    Virtual BoothBora Pharmaceuticals- Making success more certain.

    Pharma Service : API & Drug Product Development

    Bora Pharmaceuticals

    Bora's integrated small-scale and pilot capabilities directly scale to its clinical and commercial equipment, facilitating a seamless transition for clients' scale-up activities.

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    Category : Formulation Development

    Sub Category : Scale-Up Capabilities

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    Virtual BoothBora Pharmaceuticals- Making success more certain.

    Pharma Service : API & Drug Product Development

    FORMULATION SCALE UP CAPABILITIES

    Bora's integrated small-scale and pilot capabilities directly scale to its clinical and commercial equipment, facilitating a seamless transition for clients' scale-up activities.

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    Formulation Scale Up Capabilities

    Service
    Web Link

    Capabilities
    #ServicesBio

    Market
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    KEY SERVICES

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    Bora Pharmaceuticals full-view
    In-Vitro Bioequivalence studies
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    Manufacturing Vaccines
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