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    Porton Pharma Signed Strategic Partnership with Shanghai InnoStar

    24 Oct 2024

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    Porton And Genentech Publish Breakthrough In Crystallization Research

    05 Jul 2024

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    Porton Experts Join U Of Perugia's PRO-API Program For Green Chemistry

    29 Jun 2024

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    Porton Pharma Solutions Ltd. was founded in 2005, & the company's stock was successfully listed in Shenzhen Stock Exchange in 2014. Our R&D, manufacturing & operation facilities are located in China, Slovenia, the US, Belgium, Switzerland, Denmark, with more than 6000 employees worldwide. Porton leads the way with its excellent CDMO services, but also supplies APIs & intermediates for the treatment of critical diseases such as HIV/AIDS, diabetes, cancer, & influenza. Our Process Technology Centers & WHO/USFDA/EMA/PDMA/NMPA-inspected Facilities feature state-of-the-art equipment, highly flexible cGMP-compliant production assets.

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    Porton Pharma SolutionsChina Flag
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    China
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    Fangzheng Avenue, Shuitu, Beibei District, Chongqing ongqing, 401121
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    +86 02386083200
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    li.li10@portonpharma.com
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    https://www.portonpharma.com/
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    Mail ids: hong.zeng@portonpharma.com

                  leon.qin@portonpharma.com

                  Yingqiang.he1@portonpharma.com

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    CPhI India 2024

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    Product List 2023

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    GMP Certificate 2019

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    DATA COMPILATION #PharmaFlow

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    DMF filings hit all-time high in Q3 2024; China tops list with 58% increase in Type II submissions

    DMF filings hit all-time high in Q3 2024; China tops list with 58% increase in Type II submissions

    Drug Master Files, or DMFs, are confidential documents that play a crucial role in the pharmaceutical industry. These files, submitted to the US Food and Drug Administration (FDA), contain detailed information about ingredients, manufacturing processes, and packaging of medicines. They help the FDA oversee drug quality. Of the four types, Type II DMFs involve active pharmaceutical ingredients (APIs) for both branded and generic drugs. The third quarter (Q3) of 2024 saw Type II DMF submissions set a new record. A total of 309 Type II DMFs were submitted to the FDA during this period, a substantial 24.6 percent increase over Q3 2023 (with 248 submissions). The second quarter of 2024 too saw a remarkable increase, with 237 Type II DMFs being submitted compared to 178 in Q2 2023. View FDA DMF Filings in Q3 2024 (Power BI Dashboard, Free Excel Available) China witnesses steep rise in DMF submissions, beats India with maximum filings In Q3 2024, China filed 153 DMFs submissions, marking a substantial 57.7 percent increase from the 97 submissions filed in Q3 2023. India maintained its strong position but fell to the number two spot with 110 DMFs, representing a modest 3.8 percent increase from 106 in Q3 2023. The US, which came a distant third, saw a slight decline in DMF submissions, with 13 filed in Q3 2024, as compared to 18 in Q3 2023. For several years, India had a lead in Type II DMFs. Since 2020, which marked the start of the pandemic, we have noticed a gradual increase in DMFs filed by China. This year, China has surpassed India considerably in the first three quarters. During the first nine months of 2024, China submitted 372, while India filed 286 DMFs. If this lead is maintained in Q4, DMFs from China will surpass that of India in 2024.  Amongst European countries, Spain led with seven DMFs, followed by Italy at four, and Germany and the Netherlands at three each. Among other nations, Japan contributed six while Israel submitted four DMFs. In company-wise tally, China’s Jiangsu East-Mab Biomedical Technology topped the list with an impressive 14 DMFs. On its heels were Indian companies — MSN at 13 DMFs, and Vamsi Labs and Hetero Drugs at nine DMFs each. China’s Porton Pharma and Wuxi AppTec filed five, while Shanghai Keze Yongxin Biotechnology, and Qingdao Glycogene Pharmaceutical contributed four submissions each. India's Maithri Drugs also submitted four. Japanese company Santeja filed five. Overall, Asia accounted for nearly 90 percent, with China contributing a dominant 49.5 percent of all DMF submissions. India was at 35.6 percent, the US at 4.2 percent, while Europe contributed 6.5 percent.  View FDA DMF Filings in Q3 2024 (Power BI Dashboard, Free Excel Available) Diabetes, obesity, cancer, women’s health drugs emerge as hot molecules in Q3 2024 In terms of molecules, semaglutide (used for the treatment of type 2 diabetes and weight management) and relugolix (to treat prostate cancer and uterine fibroids) saw six DMF filings each in Q3 2024, indicating significant industry interest in these compounds. Following closely behind were semaglutide’s competitor tirzepatide and overactive bladder therapy vibegron, garnering four DMFs each. Finerenone (a non-steroidal drug for chronic kidney disease associated with type 2 diabetes) and voclosporin (an immunosuppressant for lupus nephritis) saw three DMFs each.  The last quarter also witnessed the introduction of 14 molecules with first-time DMFs. Among them were acetoxy empagliflozin, cabozantinib fumarate, tivozanib hydrochloride monohydrate, diosmetin, trilaciclib, clenbuterol hydrochloride, fenoterol hydrobromide, tapinarof and fezolinetant. Fezolinetant, with a DMF from Spain’s Moehs Iberica, is the active ingredient in Astellas’ Veozah, which is the first non-hormonal treatment for menopausal symptoms approved by the FDA. Tapinarof, filed by India’s Maithri Drugs, is used in Vtama, a novel steroid-free psoriasis cream. Other compounds that made their DMF debut include berotralstat, calcium phosphoryl choline chloride, phloroglucinol dihydrate, belumosudil mesylate and trimethylphloroglucinol. During Q2 2024, there were 19 drugs that saw DMF submissions for the first time, including molecules like triptorelin, sorafenib, pralsetinib, trilaciclib dihydrochloride, resmetirom (hepatology) and teneligliptin hydrochloride hydrate (metabolic disorders).  View FDA DMF Filings in Q3 2024 (Power BI Dashboard, Free Excel Available)    GDUFA fee for FY 2025: The FDA’s Generic Drug User Fee Amendments (GDUFA) is a law designed to speed access to safe and effective generic drugs to the public and reduce costs to the industry. The fiscal year 2025 fee rates were published on July 31, 2024. The FDA has revised fees under GDUFA III for all categories. While there is a slight increase in the DMF fee from US$ 94,682 in 2024 to US$ 95,084 in 2025, the ANDA fee has witnessed a significant jump — from US$ 252,453 in 2024 to US$ 321,920 in 2025. FY 2024 and FY 2025 User Fee Rates Generic drug fee category Fees rates for FY 2024 Fees rates for FY 2025 Applications: Abbreviated New Drug Application (ANDA) US$ 2,52,453   US$ 3,21,920   Drug Master File (DMF) US$ 94,682 US$ 95,084 Facilities: Active Pharmaceutical Ingredient (API)—Domestic US$ 40,464 US$ 41,580 API—Foreign US$ 55,464 US$ 56,580 Finished Dosage Form (FDF)—Domestic US$ 2,20,427   US$ 2,31,952 FDF—Foreign US$ 2,35,427   US$ 2,46,952 Contract Manufacturing Organization (CMO)—Domestic US$ 52,902 US$ 55,668 CMO—Foreign US$ 67,902 US$ 70,668 GDUFA Program: Large size operation generic drug applicant US$ 17,29,629   US$ 18,91,664 Medium size operation generic drug applicant US$ 6,91,852   US$ 7,56,666 Small business generic drug applicant US$ 1,72,963   US$ 1,89,166 Our view The highlight of the last few quarters has been the sharp rise in Type II DMF filings from China. The submission of a DMF is not required by law or any FDA regulation. FDA’s DMF guideline offers guidance on acceptable approaches to meeting regulatory requirements. Moreover, DMFs establish trust in APIs from lesser-known companies. With a growing emphasis on compliance and quality assurance, it appears that Chinese drug companies are eager to demonstrate their commitment to high standards and build trust in the US market. And that’s good news for the pharmaceutical industry.   
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    #PharmaFlow by PHARMACOMPASS
    24 Oct 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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    #PharmaFlow by PHARMACOMPASS
    08 Aug 2024
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    NEWS #PharmaBuzz

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    Porton Pharma Signed Strategic Partnership with Shanghai InnoStar
    Porton Pharma Signed Strategic Partnership with Shanghai InnoStar

    24 Oct 2024

    // PRESS RELEASE

    https://www.portonpharma.com/en/newsinfo/258.html

    PRESS RELEASE
    24 Oct 2024
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    Porton And Genentech Publish Breakthrough In Crystallization Research
    Porton And Genentech Publish Breakthrough In Crystallization Research

    05 Jul 2024

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    https://www.portonpharma.com/about-porton/news/detail.html?id=446

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    05 Jul 2024
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    Porton Experts Join U Of Perugia's PRO-API Program For Green Chemistry
    Porton Experts Join U Of Perugia's PRO-API Program For Green Chemistry

    29 Jun 2024

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    https://www.portonpharma.com/about-porton/news/detail.html?id=444

    PRESS RELEASE
    29 Jun 2024
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    Porton J-STAR Partners With ETC On Co-Processing Platform Tech Development
    Porton J-STAR Partners With ETC On Co-Processing Platform Tech Development

    28 Jun 2024

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    https://www.portonpharma.com/en/newsinfo/169.html

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    28 Jun 2024
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    Porton Will Be Participating In Biotech Outsourcing Strategies Events This June
    Porton Will Be Participating In Biotech Outsourcing Strategies Events This June

    06 Jun 2024

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    https://www.portonpharma.com/about-porton/news/detail.html?id=442

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    06 Jun 2024
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    Porton Pharma Solutions Embark On The Next Frontier In Mengeš, Slovenia
    Porton Pharma Solutions Embark On The Next Frontier In Mengeš, Slovenia

    23 May 2024

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    https://www.portonpharma.com/about-porton/news/detail.html?id=441

    PRESS RELEASE
    23 May 2024
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    ALL APIs

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    01

    Nicotine

    China

    USDMF, CEP/COS, JDMF, EU-WC, NDC, KDMF, VMF, Others

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    Pharmtech & Ingredients
    Not Confirmed
    • fda
    • EDQM
    • WHO-GMP
    Virtual BoothPorton Pharma Solutions: Value creation via innovation & discovery through technical platforms.
    USDMF arrow-down Click Us! arrow-down
    ✖

    GDUFA

    DMF Review : N/A

    Rev. Date :

    Pay. Date :

    DMF Number : 26541

    Submission : 2012-10-03

    Status : Active

    Type : II

     CEP/COS arrow-down
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    Certificate Number : R1-CEP 2012-386 - Rev 00

    Issue Date : 2019-03-11

    Type : Chemical

    Substance Number : 1452

    Status : Valid

     JDMF EU-WC NDC arrow-down
    ✖

    NDC Package Code : 75877-0002

    Start Marketing Date : 2012-02-27

    End Marketing Date : 2024-12-31

    Dosage Form (Strength) : POWDER (1kg/kg)

    Marketing Category : BULK INGREDIENT

    KDMF VMF Others AUDIT
    Porton Company Banner

    Product
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    Stock Recap
    #PipelineProspector

    Market
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    02

    Apalutamide

    China

    USDMF, CEP/COS, JDMF, EU-WC, NDC, KDMF, VMF, Others

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    Pharmtech & Ingredients
    Not Confirmed
    • fda
    • EDQM
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    GDUFA

    DMF Review : N/A

    Rev. Date :

    Pay. Date :

    DMF Number : 39029

    Submission : 2023-11-02

    Status : Active

    Type : II

     CEP/COS JDMF EU-WC NDC KDMF VMF Others AUDIT
    Porton Company Banner

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    03

    Dapagliflozin

    China

    USDMF, CEP/COS, JDMF, EU-WC, NDC, KDMF, VMF, Others

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    Pharmtech & Ingredients
    Not Confirmed
    • fda
    • EDQM
    • WHO-GMP
    Virtual BoothPorton Pharma Solutions: Value creation via innovation & discovery through technical platforms.
    USDMF arrow-down
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    GDUFA

    DMF Review : N/A

    Rev. Date :

    Pay. Date :

    DMF Number : 39028

    Submission : 2023-10-16

    Status : Active

    Type : II

     CEP/COS JDMF EU-WC NDC KDMF VMF Others AUDIT
    Porton Company Banner

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    04

    Darunavir Ethanolate

    China

    USDMF, CEP/COS, JDMF, EU-WC, NDC, KDMF, VMF, Others

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    Pharmtech & Ingredients
    Not Confirmed
    • fda
    • EDQM
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    Virtual BoothPorton Pharma Solutions: Value creation via innovation & discovery through technical platforms.
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    GDUFA

    DMF Review : N/A

    Rev. Date :

    Pay. Date :

    DMF Number : 33798

    Submission : 2019-04-22

    Status : Active

    Type : II

     CEP/COS JDMF EU-WC NDC arrow-down
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    NDC Package Code : 75877-0007

    Start Marketing Date : 2019-03-26

    End Marketing Date : 2024-12-31

    Dosage Form (Strength) : POWDER (1kg/kg)

    Marketing Category : BULK INGREDIENT

    KDMF VMF Others AUDIT
    Porton Company Banner

    Product
    Web Link

    Stock Recap
    #PipelineProspector

    Market
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    05

    Dexrazoxane

    China

    USDMF, CEP/COS, JDMF, EU-WC, NDC, KDMF, VMF, Others

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    Pharmtech & Ingredients
    Not Confirmed
    • fda
    • EDQM
    • WHO-GMP
    Virtual BoothPorton Pharma Solutions: Value creation via innovation & discovery through technical platforms.
    USDMF arrow-down
    ✖

    GDUFA

    DMF Review : N/A

    Rev. Date :

    Pay. Date :

    DMF Number : 38186

    Submission : 2023-03-17

    Status : Active

    Type : II

     CEP/COS JDMF EU-WC NDC KDMF VMF Others AUDIT
    Porton Company Banner

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    Stock Recap
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    06

    Isavuconazonium Sulfate

    China

    USDMF, CEP/COS, JDMF, EU-WC, NDC, KDMF, VMF, Others

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    Pharmtech & Ingredients
    Not Confirmed
    • fda
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    GDUFA

    DMF Review : Reviewed

    Rev. Date : 2024-09-25

    Pay. Date : 2024-08-28

    DMF Number : 39012

    Submission : 2023-11-10

    Status : Active

    Type : II

     CEP/COS JDMF EU-WC NDC KDMF VMF Others AUDIT
    Porton Company Banner

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    07

    Mefloquine

    China

    USDMF, CEP/COS, JDMF, EU-WC, NDC, KDMF, VMF, Others

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    Pharmtech & Ingredients
    Not Confirmed
    • fda
    • EDQM
    • WHO-GMP
    Virtual BoothPorton Pharma Solutions: Value creation via innovation & discovery through technical platforms.
    USDMF arrow-down
    ✖

    GDUFA

    DMF Review : N/A

    Rev. Date :

    Pay. Date :

    DMF Number : 15413

    Submission : 2001-05-04

    Status : Active

    Type : II

     CEP/COS JDMF EU-WC NDC arrow-down
    ✖

    NDC Package Code : 75877-0005

    Start Marketing Date : 2017-11-28

    End Marketing Date : 2024-12-31

    Dosage Form (Strength) : POWDER (1kg/kg)

    Marketing Category : BULK INGREDIENT

    KDMF VMF Others AUDIT
    Porton Company Banner

    Product
    Web Link

    Stock Recap
    #PipelineProspector

    Market
    Place

    08

    Nicotine

    China

    USDMF, CEP/COS, JDMF, EU-WC, NDC, KDMF, VMF, Others

    arrow
    Pharmtech & Ingredients
    Not Confirmed
    • fda
    • EDQM
    • WHO-GMP
    Virtual BoothPorton Pharma Solutions: Value creation via innovation & discovery through technical platforms.
    USDMF arrow-down
    ✖

    GDUFA

    DMF Review : N/A

    Rev. Date :

    Pay. Date :

    DMF Number : 38020

    Submission : 2023-02-10

    Status : Active

    Type : II

     CEP/COS JDMF EU-WC NDC arrow-down
    ✖

    NDC Package Code : 75877-0002

    Start Marketing Date : 2012-02-27

    End Marketing Date : 2024-12-31

    Dosage Form (Strength) : POWDER (1kg/kg)

    Marketing Category : BULK INGREDIENT

    KDMF VMF Others AUDIT
    Porton Company Banner

    Product
    Web Link

    Stock Recap
    #PipelineProspector

    Market
    Place

    09

    Salmeterol Xinafoate

    China

    USDMF, CEP/COS, JDMF, EU-WC, NDC, KDMF, VMF, Others

    arrow
    Pharmtech & Ingredients
    Not Confirmed
    • fda
    • EDQM
    • WHO-GMP
    Virtual BoothPorton Pharma Solutions: Value creation via innovation & discovery through technical platforms.
    USDMF arrow-down
    ✖

    GDUFA

    DMF Review : N/A

    Rev. Date :

    Pay. Date :

    DMF Number : 37070

    Submission : 2022-05-23

    Status : Active

    Type : II

     CEP/COS JDMF EU-WC NDC KDMF VMF Others AUDIT
    Porton Company Banner

    Product
    Web Link

    Stock Recap
    #PipelineProspector

    Market
    Place

    10

    Sulfanilamide

    China

    USDMF, CEP/COS, JDMF, EU-WC, NDC, KDMF, VMF, Others

    arrow
    Pharmtech & Ingredients
    Not Confirmed
    • fda
    • EDQM
    • WHO-GMP
    Virtual BoothPorton Pharma Solutions: Value creation via innovation & discovery through technical platforms.
    USDMF arrow-down
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    GDUFA

    DMF Review : N/A

    Rev. Date :

    Pay. Date :

    DMF Number : 35714

    Submission : 2021-05-19

    Status : Active

    Type : II

     CEP/COS JDMF EU-WC NDC KDMF VMF Others AUDIT
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    KEY PRODUCTS

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    Services

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    API Manufacturing

    Discover their expertise for : API Manufacturing

    Drug Product Manufacturing

    Discover their expertise for : Drug Product Manufacturing

    Injectable / Parenteral

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    01

    INJECTABLE FORMULATION CONTRACT ...

    China
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    Medlab Asia & Asia Health
    Not Confirmed
    • fda
    • EDQM
    • WHO-GMP

    Virtual BoothPorton Pharma Solutions: Value creation via innovation & discovery through technical platforms.

    Pharma Service : Drug Product Manufacturing

    Porton Pharma Solutions

    Porton Pharma has a cGMP drug product manufacturing site in Chongqing, China that offers ampoules and vials for powder and liquids from pilot and clinical trial scale to commercial scale.

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    Category : Injectable / Parenteral

    Sub Category : Others

    • fda
    • EDQM
    • WHO-GMP

    Virtual BoothPorton Pharma Solutions: Value creation via innovation & discovery through technical platforms.

    Pharma Service : Drug Product Manufacturing

    INJECTABLE FORMULATION CONTRACT MANUFACTURING

    Porton Pharma has a cGMP drug product manufacturing site in Chongqing, China that offers ampoules and vials for powder and liquids from pilot and clinical trial scale to commercial scale.

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    Injectable Formulation Contract Manufacturing

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    02

    POTENT INJECTABLE FORMULATIONS

    China
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    Medlab Asia & Asia Health
    Not Confirmed
    • fda
    • EDQM
    • WHO-GMP

    Virtual BoothPorton Pharma Solutions: Value creation via innovation & discovery through technical platforms.

    Pharma Service : Drug Product Manufacturing

    Porton Pharma Solutions

    Porton Pharma is a contract manufacturer of potent injectable formulations such as vials (aseptic) and ampoules filled with liquid and lyo powder.

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    Category : Injectable / Parenteral

    Sub Category : High Potency APIs (HPAPIs)

    • fda
    • EDQM
    • WHO-GMP

    Virtual BoothPorton Pharma Solutions: Value creation via innovation & discovery through technical platforms.

    Pharma Service : Drug Product Manufacturing

    POTENT INJECTABLE FORMULATIONS

    Porton Pharma is a contract manufacturer of potent injectable formulations such as vials (aseptic) and ampoules filled with liquid and lyo powder.

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    Potent Injectable Formulations

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    Capsule

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    01

    CONTRACT MANUFACTURING FOR CAPSU...

    China
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    Fi Europe 2024
    Not Confirmed
    • fda
    • EDQM
    • WHO-GMP

    Virtual BoothPorton Pharma Solutions: Value creation via innovation & discovery through technical platforms.

    Pharma Service : Drug Product Manufacturing

    Porton Pharma Solutions

    Porton Pharma is a contract development and manufacturing organization (CDMO) that has small molecule drug product manufacturing capabilities for modified release, immediate release, and micro-pellet filled capsules.

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    Category : Capsule

    Sub Category : Overview

    • fda
    • EDQM
    • WHO-GMP

    Virtual BoothPorton Pharma Solutions: Value creation via innovation & discovery through technical platforms.

    Pharma Service : Drug Product Manufacturing

    CONTRACT MANUFACTURING FOR CAPSULES

    Porton Pharma is a contract development and manufacturing organization (CDMO) that has small molecule drug product manufacturing capabilities for modified release, immediate release, and micro-pellet filled capsules.

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    Contract Manufacturing for Capsules

    Service
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    Capabilities
    #ServicesBio

    Market
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    02

    CONTRACT MANUFACTURING FOR POTEN...

    China
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    Fi Europe 2024
    Not Confirmed
    • fda
    • EDQM
    • WHO-GMP

    Virtual BoothPorton Pharma Solutions: Value creation via innovation & discovery through technical platforms.

    Pharma Service : Drug Product Manufacturing

    Porton Pharma Solutions

    Porton Pharma has the capability for the contract development and manufacturing of potent capsules from its cGMP drug product manufacturing site based in Chongqing China.

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    Category : Capsule

    Sub Category : High Potency APIs (HPAPIs)

    • fda
    • EDQM
    • WHO-GMP

    Virtual BoothPorton Pharma Solutions: Value creation via innovation & discovery through technical platforms.

    Pharma Service : Drug Product Manufacturing

    CONTRACT MANUFACTURING FOR POTENT CAPSULES

    Porton Pharma has the capability for the contract development and manufacturing of potent capsules from its cGMP drug product manufacturing site based in Chongqing China.

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    Contract Manufacturing for Potent Capsules

    Service
    Web Link

    Capabilities
    #ServicesBio

    Market
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    03

    IMMEDIATE & MODIFIED RELEASE CAP...

    China
    Contact Supplier
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    Fi Europe 2024
    Not Confirmed
    • fda
    • EDQM
    • WHO-GMP

    Virtual BoothPorton Pharma Solutions: Value creation via innovation & discovery through technical platforms.

    Pharma Service : Drug Product Manufacturing

    Porton Pharma Solutions

    Porton Pharma is engaged in the contract manufacturing of immediate release, modified release, and micro-pellet filled capsules for clinical and commercial scales.

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    Category : Capsule

    Sub Category : Controlled / Immediate / Modified Release

    • fda
    • EDQM
    • WHO-GMP

    Virtual BoothPorton Pharma Solutions: Value creation via innovation & discovery through technical platforms.

    Pharma Service : Drug Product Manufacturing

    IMMEDIATE & MODIFIED RELEASE CAPSULES

    Porton Pharma is engaged in the contract manufacturing of immediate release, modified release, and micro-pellet filled capsules for clinical and commercial scales.

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    Immediate & Modified Release Capsules

    Service
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    Capabilities
    #ServicesBio

    Market
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    API & Drug Product Development

    Discover their expertise for : API & Drug Product Development

    Inspections and registrations

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    ABOUT THIS PAGE

    Contact Porton Pharma Solutions and get a quotation

    Porton Pharma Solutions is a supplier offers 32 products (APIs, Excipients or Intermediates).

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