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    About

    Zhejiang Huahai Pharmaceuticals Co., Ltd.was initially founded in 1989, and the company's stock was successfully listed in Shanghai Stock Exchange in March, 2003. Huahai Pharmaceuticals, a large scaled modern pharmaceutical group that integrates fomulations, APIs(Active Pharmaceutical Ingredients) and intermediates, is developing both domestic and international markets, and performing parallel development of science, industry...
    Zhejiang Huahai Pharmaceuticals Co., Ltd.was initially founded in 1989, and the company's stock was successfully listed in Shanghai Stock Exchange in March, 2003. Huahai Pharmaceuticals, a large scaled modern pharmaceutical group that integrates fomulations, APIs(Active Pharmaceutical Ingredients) and intermediates, is developing both domestic and international markets, and performing parallel development of science, industry and commerce. With a total asset of 1,900 million yuan, the company has 11branches (subsidiaries) in the United States, Shanghai, Hangzhou, and Linhai.

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    Zhejiang Huahai PharmaceuticalChina Flag
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    Xunqiao, Linhai, Zhejiang 317024
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    +86-576-85016116
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    enquiries@pharmacompass.com
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    https://en.huahaipharm.com:443/
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    INTERVIEW #SpeakPharma

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    “Translational Pharmaceutics, our flagship platform for drug development, empowers our clients with unparalleled flexibility”

    “Translational Pharmaceutics, our flagship platform for drug development, empowers our clients with unparalleled flexibility”

    This week, SpeakPharma interviews Denise Sutton, Chief Operating Officer and Site Head at Quotient Sciences’ Nottingham facility in the UK. Quotient Sciences is a drug development and manufacturing accelerator that offers the innovative Translational Pharmaceutics platform to support customers in overcoming drug development challenges. Sutton has been with the company for over 25 years. In this interview, she provides insights into the evolution of Quotient Sciences’ Nottingham facility and discusses how the organization has transformed from a small 10-bed clinic to a comprehensive drug development campus with six GMP suites. She also shares her perspective on the company’s unique approach to integrating drug development services. HIGHLIGHTS// evolution of Quotient Sciences’ Nottingham facility/ unique approach to integrating drug development services How has the Nottingham site transformed from when it was founded, to what it is today? Initially, we were a small company with fewer than 50 employees, a 10-bed clinic, and a single lab. Over 90 percent of our work focused on gamma scintigraphic imaging (a diagnostic test that creates images of the body’s internal organs and tissues using gamma rays). Due to the short half-life radionuclides we used to label dosage forms, every product we manufactured had a limited time to be dosed. At the end of 1999, we moved our headquarters to a purpose-built, two-storey facility—now known as Trent House on our now much larger Nottingham campus. We built three good manufacturing practice (GMP) suites on the top floor and three clinical wards on the bottom floor. These were very early days that marked the start of our Translational Pharmaceutics platform. We continued to expand the range of scintigraphy applications we offered in response to changing customer requirements until, in 2008, when we approached the MHRA (UK’s Medicines and Healthcare products Regulatory Agency) with a new request. We asked if it might be possible to work at the same pace as we did in our scintigraphic imaging studies, but do so for conventional drug development, without the radiolabel. We explored the application of ICH Q8 Quality by Design (QbD) guidelines to introduce a compositional design space into the CMC section of our regulatory dossier. This officially created a methodology for applying the Translational Pharmaceutics platform, and we haven't looked back since. Today, we have expanded substantially. Our Nottingham site is a campus of five buildings. We have development and analytical labs, six GMP suites, six clinical wards with a total of 85 beds (where we conduct healthy volunteer phase 1 clinical studies), and many talented colleagues covering our spectrum of CRO and CDMO services. HIGHLIGHTS// officially created a methodology for applying the Translational Pharmaceutics platform/ development and analytical labs/ six GMP suites   How is Translational Pharmaceutics applied to drug development programs? We apply Translational Pharmaceutics across three core applications: first-in-human clinical studies, drug product optimization programs through rapid formulation development and clinical testing, and as a part of human ADME (absorption, distribution, metabolism, and excretion) programs. No matter how a client chooses to work with us to apply Translational Pharmaceutics, the benefits of using a single organization and project management team to integrate services lets our clients remain in control and one step ahead of the emerging data that impacts the success of their molecule. Over all these years, our flagship Translational Pharmaceutics platform for drug development has remained unchanged in the way it empowers our customers and offers them unparalleled flexibility. HIGHLIGHTS// three core applications/ benefits of using a single organization/ clients remain in control   What would you say are the key strengths of Quotient Sciences’ Nottingham site? How do you support customer programs? Nowhere else would a single project manager oversee such a broad spectrum of activities, let alone be expected to ensure seamless, timely progression across functions that in any other company (i.e. at other CDMOs or CROs) would be delivered through multiple operating areas or through the use of a combination of third-party vendors. The project managers do face challenges. But by working with the project team, they are able to anticipate, avoid, and mitigate any impact whenever necessary. We know that time is incredibly valuable for our customers. A project Gantt chart is our project management team’s guiding light. I believe our project management team is truly world-leading – they communicate well, show great compassion, and lead with integrity. I’m super proud of our high-performing, supportive, cross-functional teams that support our customers when they trust their molecules to us, and work collaboratively to deliver the best possible service. After 25 years at Quotient, I continue to really enjoy going to work. I am indebted to various colleagues for helping me continue to feel this way. HIGHLIGHTS// project management team is truly world-leading/ high-performing, supportive, cross-functional teams/ 25 years at Quotient  

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    16 Dec 2024
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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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    Impressions: 421

    https://www.pharmacompass.com/radio-compass-blog/cdmo-activity-tracker-bora-polpharma-make-acquisitions-evonik-euroapi-porton-announce-technological-expansions

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    NEWS #PharmaBuzz

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    Pfizer tabs controversial Chinese firm Huahai to make Paxlovid
    Pfizer tabs controversial Chinese firm Huahai to make Paxlovid

    24 Aug 2022

    // Kevin Dunleavy FIERCEPHARMA

    https://www.fiercepharma.com/manufacturing/paxlovid-production-pfizer-partners-chinese-company-huahai-which-coming-fda-ban

    Kevin Dunleavy FIERCEPHARMA
    24 Aug 2022
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    Pfizer Picks China Firm Involved in Drug Recall for Covid Pill
    Pfizer Picks China Firm Involved in Drug Recall for Covid Pill

    23 Aug 2022

    // BLOOMBERG

    https://www.bnnbloomberg.ca/pfizer-picks-china-firm-involved-in-drug-recall-for-covid-pill-1.1809083

    BLOOMBERG
    23 Aug 2022
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    Biocon-Viatris, AstraZeneca, Huhai and more—Fierce Pharma Asia
    Biocon-Viatris, AstraZeneca, Huhai and more—Fierce Pharma Asia

    19 Nov 2021

    // Angus Liu FIERCEPHARMA

    https://www.fiercepharma.com/pharma-asia/biocon-viatris-insulin-biosimilar-astrazeneca-china-performance-huahai-fda-warning-lift

    Angus Liu FIERCEPHARMA
    19 Nov 2021
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    Valsartan recall protagonist comes off FDA warning letter
    Valsartan recall protagonist comes off FDA warning letter

    16 Nov 2021

    // Angus Liu FIERCEPHARMA

    https://www.fiercepharma.com/manufacturing/3-years-valsartan-recall-zhejiang-huahai-china-drug-manufacturer-fda-warning-letter

    Angus Liu FIERCEPHARMA
    16 Nov 2021
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    Zhejiang Huahai Pharma Receives FDA Warning Letter
    Zhejiang Huahai Pharma Receives FDA Warning Letter

    11 Nov 2021

    // FDA

    https://www.pharmacompass.com/pdf/news/zhejiang-huahai-pharma-receives-fda-warning-letter-1637048144.pdf

    FDA
    11 Nov 2021
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    EMA, FDA begin reviewing heartburn medicines for carcinogen
    EMA, FDA begin reviewing heartburn medicines for carcinogen

    17 Sep 2019

    // Zachary Brennan ENDPTS

    https://endpts.com/ema-fda-begin-reviewing-heartburn-medicines-for-carcinogen/

    Zachary Brennan ENDPTS
    17 Sep 2019
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    Zhejiang Huahai Pharmaceutical

    Registration Number : 304MF10122

    Registrant's Address : Xunqiao, Linhai, Zhejiang 317024, China

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    Zhejiang Huahai Pharmaceutical

    Registration Number : 227MF10237

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    Initial Date of Registration : 2015-09-24

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    Zhejiang Huahai Pharmaceutical

    Registration Number : 227MF10268

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    Zhejiang Huahai Pharmaceutical

    Registration Number : 303MF10128

    Registrant's Address : Xunqiao, Linhai, Zhejiang 317024, China

    Initial Date of Registration : 2021-08-16

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    Zhejiang Huahai Pharmaceutical

    Registration Number : 228MF10003

    Registrant's Address : Xunqiao, Linhai, Zhejiang 317024, China

    Initial Date of Registration : 2016-01-08

    Latest Date of Registration : 2016-01-08

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    Zhejiang Huahai Pharmaceutical

    Registration Number : 306MF10094

    Registrant's Address : Xunqiao, Linhai, Zhejiang 317024, China

    Initial Date of Registration : 2024-07-11

    Latest Date of Registration : 2024-07-11

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    Zhejiang Huahai Pharmaceutical

    Registration Number : 301MF10091

    Registrant's Address : Xunqiao, Linhai, Zhejiang 317024, China

    Initial Date of Registration : 2019-11-15

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    Zhejiang Huahai Pharmaceutical

    Registration Number : 219MF10148

    Registrant's Address : Xunqiao, Linhai, Zhejiang 317024, China

    Initial Date of Registration : 2007-04-27

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    Zhejiang Huahai Pharmaceutical

    Registration Number : 303MF10094

    Registrant's Address : Xunqiao, Linhai, Zhejiang 317024, China

    Initial Date of Registration : 2021-06-15

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    Inspections and registrations

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    District Decision : No Action Indicated

    Inspection End Date : 2010-09-02

    Zhejiang Huahai Pharmaceutical

    City : Linhai,

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    Country/Area : CN

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    District : ORA

    Center : CDER

    Project Area : Drug Quality Assurance

    District Decision : No Action Indicated

    Inspection End Date : 2010-09-02

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    District Decision : No Action Indicated

    Inspection End Date : 2010-09-08

    Zhejiang Huahai Pharmaceutical

    City : Duqiao, Linhai City

    State :

    Country/Area : CN

    Zip :

    District : ORA

    Center : CDER

    Project Area : Drug Quality Assurance

    District Decision : No Action Indicated

    Inspection End Date : 2010-09-08

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    District Decision : No Action Indicated

    Inspection End Date : 2013-08-09

    Zhejiang Huahai Pharmaceutical

    City : Linhai,

    State :

    Country/Area : CN

    Zip :

    District : ORA

    Center : CDER

    Project Area : Drug Quality Assurance

    District Decision : No Action Indicated

    Inspection End Date : 2013-08-09

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    FDA Audited

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    District Decision : No Action Indicated

    Inspection End Date : 2014-05-23

    Zhejiang Huahai Pharmaceutical

    City : Duqiao, Linhai City

    State :

    Country/Area : CN

    Zip :

    District : ORA

    Center : CDER

    Project Area : Drug Quality Assurance

    District Decision : No Action Indicated

    Inspection End Date : 2014-05-23

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    FDA Audited

    USA
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    Pharma, Lab & Chemical Expo
    Not Confirmed

    District Decision : No Action Indicated

    Inspection End Date : 2015-03-27

    Zhejiang Huahai Pharmaceutical

    City : Linhai,

    State :

    Country/Area : CN

    Zip :

    District : ORA

    Center : CDER

    Project Area : Drug Quality Assurance

    District Decision : No Action Indicated

    Inspection End Date : 2015-03-27

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    06

    FDA Audited

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    Not Confirmed
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    FDA Audited

    USA
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    Pharma, Lab & Chemical Expo
    Not Confirmed

    District Decision : Voluntary Action Indicated

    Inspection End Date : 2017-05-19

    Zhejiang Huahai Pharmaceutical

    City : Duqiao

    State :

    Country/Area : CN

    Zip :

    District : ORA

    Center : CDER

    Project Area : Drug Quality Assurance

    District Decision : Voluntary Action Indicated

    Inspection End Date : 2017-05-19

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    EDQM

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    GMP Certified

    EU
    Antibody Engineering
    Not Confirmed
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    GMP Certified

    EU
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    Antibody Engineering
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    Zhejiang Huahai Pharmaceutical

    Type : GMP Certificates

    Number : 2007/HMP/PT...

    EudraGMDP Key : 8767

    Country : China

    Issue Date :

    Post Code : 317024

    NCA Ref : A058 3020 84...

    City : LINHAI, PROVINCE ZHEJIA...

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    02

    GMP Certified

    EU
    Antibody Engineering
    Not Confirmed
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    GMP Certified

    EU
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    Antibody Engineering
    Not Confirmed

    Zhejiang Huahai Pharmaceutical

    Type : GMP Certificates

    Number : ES/137/11

    EudraGMDP Key : 11558

    Country : China

    Issue Date :

    Post Code : 317024

    NCA Ref : 405

    City : Zhejiang China

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    GMP Certified

    EU
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    Not Confirmed
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    GMP Certified

    EU
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    Antibody Engineering
    Not Confirmed

    Zhejiang Huahai Pharmaceutical

    Type : GMP Certificates

    Number : ES/123/11

    EudraGMDP Key : 11560

    Country : China

    Issue Date :

    Post Code : 317024

    NCA Ref : 404

    City : Zhejiang China

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    04

    GMP Certified

    EU
    Antibody Engineering
    Not Confirmed
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    GMP Certified

    EU
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    Antibody Engineering
    Not Confirmed

    Zhejiang Huahai Pharmaceutical

    Type : GMP Certificates

    Number : ES/033/12

    EudraGMDP Key : 11560

    Country : China

    Issue Date :

    Post Code : 317024

    NCA Ref : 404

    City : Zhejiang China

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    05

    GMP Certified

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    Not Confirmed
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    GMP Certified

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    Not Confirmed

    Zhejiang Huahai Pharmaceutical

    Type : GMP Certificates

    Number : ES/029/12

    EudraGMDP Key : 11560

    Country : China

    Issue Date :

    Post Code : 317024

    NCA Ref : 404

    City : Zhejiang China

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    06

    GMP Certified

    EU
    Antibody Engineering
    Not Confirmed
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    GMP Certified

    EU
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    Antibody Engineering
    Not Confirmed

    Zhejiang Huahai Pharmaceutical

    Type : GMP Certificates

    Number : ES/030/12

    EudraGMDP Key : 11560

    Country : China

    Issue Date :

    Post Code : 317024

    NCA Ref : 404

    City : Zhejiang China

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    07

    GMP Certified

    EU
    Antibody Engineering
    Not Confirmed
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    GMP Certified

    EU
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    Antibody Engineering
    Not Confirmed

    Zhejiang Huahai Pharmaceutical

    Type : GMP Certificates

    Number : ES/031/12

    EudraGMDP Key : 11560

    Country : China

    Issue Date :

    Post Code : 317024

    NCA Ref : 404

    City : Zhejiang China

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    08

    GMP Certified

    EU
    Antibody Engineering
    Not Confirmed
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    GMP Certified

    EU
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    Antibody Engineering
    Not Confirmed

    Zhejiang Huahai Pharmaceutical

    Type : GMP Certificates

    Number : DE_HH_01_GM...

    EudraGMDP Key : 26737

    Country : China

    Issue Date :

    Post Code : 317016

    NCA Ref : 20742

    City : Zhejiang

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    09

    GMP Certified

    EU
    Antibody Engineering
    Not Confirmed
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    GMP Certified

    EU
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    Antibody Engineering
    Not Confirmed

    Zhejiang Huahai Pharmaceutical

    Type : GMP Certificates

    Number : DE_HH_01_GM...

    EudraGMDP Key : 30108

    Country : China

    Issue Date : 2016-02-04

    Post Code : 317024

    NCA Ref : 00021462

    City : Zhejiang

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    10

    GMP Certified

    EU
    Antibody Engineering
    Not Confirmed
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    GMP Certified

    EU
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    Antibody Engineering
    Not Confirmed

    Zhejiang Huahai Pharmaceutical

    Type : GMP Certificates

    Number : DE_HH_01_GM...

    EudraGMDP Key : 30108

    Country : China

    Issue Date : 2015-09-01

    Post Code : 317024

    NCA Ref : 00021462

    City : Zhejiang

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    GDUFA

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    01

    GDUFA fees paid

    USA
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    Not Confirmed
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    GDUFA fees paid

    USA
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    Pharma, Lab & Chemical Expo
    Not Confirmed
    • fda
    • EDQM
    • WHO-GMP
    Virtual Booth Boost your online visibility by uploading your products, APIs, FDFs, intermediates, excipients, and services for free on PharmaCompass. Rank higher among suppliers and expand your reach across the internet efficiently and cost-effectively.

    Paid in : 2019

    Zhejiang Huahai Pharmaceutical

    API Manufacturer : API MANUFACTURE

    FDF Manufacturer : FDF MANUFACTURE

    Facility Name : Zhejiang Huahai Pharmaceutical...

    Business Address : Xunqiao Linhai Zhejiang 3170...

    FEI Number : 3003999190

    Country : China

    Paid in : 2019

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    02

    GDUFA fees paid

    USA
    Pharma, Lab & Chemical Expo
    Not Confirmed
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    GDUFA fees paid

    USA
    arrow
    Pharma, Lab & Chemical Expo
    Not Confirmed
    • fda
    • EDQM
    • WHO-GMP
    Virtual Booth Boost your online visibility by uploading your products, APIs, FDFs, intermediates, excipients, and services for free on PharmaCompass. Rank higher among suppliers and expand your reach across the internet efficiently and cost-effectively.

    Paid in : 2019

    Zhejiang Huahai Pharmaceutical

    API Manufacturer : API MANUFACTURE

    FDF Manufacturer :

    Facility Name : Zhejiang Huahai Pharmaceutical...

    Business Address : Coastal Industrial Zone Duqi...

    FEI Number : 3003885745

    Country : China

    Paid in : 2019

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    ABOUT THIS PAGE

    Contact Zhejiang Huahai Pharmaceutical and get a quotation

    Zhejiang Huahai Pharmaceutical is a supplier offers 107 products (APIs, Excipients or Intermediates).

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