Douglas CDMO | Digital Content

Efficient pathways Regulatory Edge Of New Zealand For Pharma Devp

15 Jul 2024

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Smart softgels: driving innovation in pharma

21 Jun 2024

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CRO, CMO, and CDMO partnerships: A guide for pharma and biotech companies

05 Jun 2024

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DATA COMPILATION
#PharmaFlow

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Website

CPhI Worldwide, Milan

Booth #22A18

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DIGITAL CONTENT

2 CORPORATE CONTENT #SupplierSpotlight, 1 DATA COMPILATION #PharmaFlow, 27 NEWS #PharmaBuzz

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2 CORPORATE CONTENT #SupplierSpotlight
1 DATA COMPILATION #PharmaFlow
27 NEWS #PharmaBuzz

DEVELOPMENTS

3 Drugs in Development

3 Drugs in Development

FINISHED DOSAGE FORMULATIONS

40 FDF Dossiers, 40 Listed Dossiers

40 FDF Dossiers
40 Listed Dossiers

SERVICES

Packaging, Drug Product Manufacturing, API & Drug Product Development

pharmaServices
Packaging
- 1 Clinical Services
- 1 Contract Services
Drug Product Manufacturing
API & Drug Product Development
- 11 Formulation Development

KEY SERVICES

Tablet Contract Manufacturing, Modified Release Tablet Manufacturing, Manufacturing of Coated Tablets, Contract Manufacturing for Hard Capsules, Softgel Contract Manufacturing, Modified Release Formulation Development, Contract Manufacturer for Chewable Tablets, Highly Potent Drug Product Manufacturing, Clinical Manufacturing of Tablets, Clinical Supply of Capsules

Tablet Contract Manufacturing
Modified Release Tablet Manufacturing
Manufacturing of Coated Tablets
Contract Manufacturing for Hard Capsules
Softgel Contract Manufacturing
Modified Release Formulation Development
Contract Manufacturer for Chewable Tablets
Highly Potent Drug Product Manufacturing
Clinical Manufacturing of Tablets
Clinical Supply of Capsules

INSPECTIONS & REGISTRATIONS

1 FDA, 1 GDUFA

inspections
1 FDA
1 GDUFA

Douglas CDMO develops, manufactures, and packs various dosage forms, and provides regulatory support for international distribution.

About

Douglas CDMO helps pharma and biotech innovators achieve competitive advantages in cost, speed, and quality. With our expertise, technology and global distribution footprint, we assist from development through to distribution. Our two cGMP manufacturing sites are situated in beautiful Auckland, New Zealand, and Nadi, Fiji. We produce consumer healthcare products and prescription drugs for medical classifications such as oncology, dermatology, and the central nervous system, and have deep Softgel formulation expertise. We take pride in our reputation as a partner that is easy to work with. Contact our team of experts. We are happy to help.

CPhI Worldwide, MilanCPhI Worldwide, Milan

Industry Trade Show

Booth #22A18

08-10 October, 2024

Fiera Milano, Italy
Bio-Europe 2024Bio-Europe 2024

Industry Trade Show

Attending

04-06 November, 2024

Stockholm, Sweden
American Pharma SummitAmerican Pharma Summit

Industry Trade Show

Attending

18-19 November, 2024

The Westin Copley Place - Boston, MA

CONTACT DETAILS

Click the arrow to open the dropdown

Country

New Zealand

Address

2 Te Pai Pl Henderson Auckland 0610

Telephone

+64 98350660

cdmo@douglas.co.nz

Website

https://www.douglascdmo.com/

https://www.linkedin.com/company/douglas-pharmaceuticals/

YouTube

http://www.youtube.com/@douglaspharmaceuticals9647

Digital content

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CORPORATE CONTENT #SupplierSpotlight

EV-54 Nano Vial Filling Machine

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Corporate Video

DATA COMPILATION #PharmaFlow

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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// PRESS RELEASE

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// PRESS RELEASE

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05 Jun 2024

// PRESS RELEASE

Bespoke client solutions: A personalized approach as a privately owned CDMO

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Softgels Address Stability, Shelf-Life, And Bioavailability In Drug Formulation

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The case for softgels: Addressing stability, shelf-life, & bioavailability

26 Apr 2024

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Drugs in Development

01 Douglas CDMO

New Zealand

CPhI Worldwide, Milan

Booth #22A18

Douglas CDMO develops, manufactures, and packs various dosage forms, and provides regulatory support for international distribution.

Lead Product(s) : Ketamine Hydrochloride

Therapeutic Area : Psychiatry/Psychology

Highest Development Status : Phase II

Partner/Sponsor/Collaborator : Not Applicable

Deal Size : Not Applicable

Deal Type : Not Applicable

DEALS_DEV

Douglas Pharmaceuticals Announces Formation of Clinical Advisory Board for Lead Program R-107

Details : R-107, an oral extended-release dose of racemic ketamine being developed as add-on or monotherapy for treatment resistant depression (TRD). It has demonstrated a significant antidepressant effect with maintenance of response at 3 months, high compliance ...

Brand Name : R-107

Molecule Type : Small molecule

Upfront Cash : Not Applicable

January 26, 2023

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Virtual Booth

02 Douglas CDMO

New Zealand

CPhI Worldwide, Milan

Booth #22A18

Douglas CDMO develops, manufactures, and packs various dosage forms, and provides regulatory support for international distribution.

Lead Product(s) : Isotretinoin

Therapeutic Area : Dermatology

Highest Development Status : Approved

Recipient : Upsher-Smith Laboratories

Deal Size : Not Applicable

Deal Type : Not Applicable

DEALS_DEV

Upsher-Smith Launches Isotretinoin Capsules

Details : Upsher-Smith's product is AB2-rated to the branded product, Absorica® (isotretinoin) capsules. Isotretinoin capsules are a generic version of ABSORICA® indicated for the treatment of severe recalcitrant nodular acne.

Brand Name : Isotretinoin-Generic

Molecule Type : Small molecule

Upfront Cash : Not Applicable

June 25, 2021

Stock Recap
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03 Douglas CDMO

New Zealand

CPhI Worldwide, Milan

Booth #22A18

Douglas CDMO develops, manufactures, and packs various dosage forms, and provides regulatory support for international distribution.

Lead Product(s) : Ketamine Hydrochloride

Therapeutic Area : Psychiatry/Psychology

Highest Development Status : Phase II

Partner/Sponsor/Collaborator : Not Applicable

Deal Size : Not Applicable

Deal Type : Not Applicable

DEALS_DEV

Trial Data Suggests Major Breakthrough in Treatment Resistant Depression

Details : R-107 (extended-release oral dose of ketamine) act as a blocks the NMDA receptor and it is investigated for the treatment of treatment resistant depression.

Brand Name : R-107

Molecule Type : Small molecule

Upfront Cash : Not Applicable

June 15, 2021

Stock Recap
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Data Compilation
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Virtual Booth