Dongying Tiandong Pharmaceutical Co., Ltd. DMF, CEP, Written Confirmations, FDF, Prices, Patents, Patents & Exclusivities, Dossier, Manufacturer, Licensing, Distributer, Suppliers, News, GMP

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INTERVIEW #SpeakPharma, VLOG #PharmaReel, DATA COMPILATION #PharmaFlow, 4 NEWS #PharmaBuzz

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INTERVIEW #SpeakPharma
VLOG #PharmaReel
DATA COMPILATION #PharmaFlow
4 NEWS #PharmaBuzz

ACTIVE PHARMA INGREDIENTS

3 All APIs, 3 USDMF, 1 CEP/COS, 2 KDMF, 2 NDC API, 1 Listed APIs

3 All APIs
3 USDMF
1 CEP/COS
2 KDMF
2 NDC API
1 Listed APIs

INSPECTIONS & REGISTRATIONS

1 FDA, 2 EDQM

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2 EDQM

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About

Dongying Tiandong Pharmaceutical Co.,ltd founded in 1992, subordinated to Shandong Haike Chemical Group, is located in Dongying city, the center area of Yellow River Delta High-efficiency Ecological Economic Zone and Shandong Peninsula Blue Economic Zone, specially engaging in development, production and sales of polysaccharide products. The company is entitled as High and New Tech Enterprise in ShandongProvince. The company focuses on low-molecular weight heparins, heparin sodium and heparin calcium and so on, as the biggest low-molecular weight heparin API manufacturer in China. The injection workshop has been built with annual capacity of 21 million units of aqueous solution injections, which makes the company to have the complete industry chain from API to injection product and updates the heparin industry chain. Tiandong company is the only one to pass EDQM inspection, granted COS for enoxapairn sodium in China. Moreover, its enoxaparin sodium has been granted with Brazil GMP certificate, Swedish GMP certificate and French GMP certificate successively, and completed the registrations in many other countries and regions, and has been exported to more than forty countries in the world. The company keeps long-term close partnership with School of Pharmaceutical Sciences, ShandongUniversity, which strengthens our innovative ability of R & D. The company has applied 15 invention patents or utility model patents associated with heparin products. In 2009, the company has undertaken the national Major Creation of new drugs project on Quality Standards Study and Establishment of Five Low Molecular Weight Heparins. Over 20 years, the company has always made efforts to provide better pharmaceutical products and services for people, and established impeccable production service management system and quality management system by years of practices and innovation to assure product quality and the interests of clients.

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03-05 January, 2025

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CONTACT DETAILS

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Country

China

Address

Address: No. 1236, Nan-er Road, Dongying, Shandong, China

Telephone

+86-546-7791092

enquiries@pharmacompass.com

Website

https://en.td-pharm.com/

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INTERVIEW #SpeakPharma

[Sponsored by another company]

“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

Impressions: 4566

VLOG #PharmaReel

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Full-Service Generic API Company

DATA COMPILATION #PharmaFlow

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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.

Impressions: 365

NEWS #PharmaBuzz

Dongying Tiandong Receives FDA Warning Letter

10 Nov 2016

// FDA

French raises concerns about heparin made by Dongying Tiandong

01 Mar 2016

// Gareth MacDonald+ IN PHARMATECHNOLOGIST

Potentially tainted heparin from China uncovered by French regulators

29 Feb 2016

// Eric Palmer FIERCE PHARMA MANUFATURING

Dongying Tiandong Pharmaceutical Co., Ltd fails EDQM Inspection

25 Feb 2016

// EDQM

ALL APIs

Click the button for full data set

01

Enoxaparin Sodium

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

Antibody Engineering

Not Confirmed

02

Heparin Sodium

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

Antibody Engineering

Not Confirmed

03

Dalteparin sodium

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

Antibody Engineering

Not Confirmed

FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]

USDMF

FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]

CEP/COS

FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]

KDMF

01

Heparin sodium

China

Antibody Engineering

Not Confirmed

02

Heparin sodium

China

Antibody Engineering

Not Confirmed

FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]

NDC API

01

ENOXAPARIN SODIUM

China

Antibody Engineering

Not Confirmed

02

HEPARIN SODIUM

China

Antibody Engineering

Not Confirmed

Only 10 entries up to this point, click to access all

LISTED APIs

Dongying Tiandong Pharmaceutical Co., Ltd.

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.

Dalteparin sodium

Product
Web Link

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Market
Place

About the Company

Dongying Tiandong Pharmaceutical Co.,ltd founded in 1992, subordinated to Shandong Haike Chemical Group, is located in Dongying city, the center area of Yellow River Delta High-efficiency Ecological Economic Zone and Shandong Peninsula Blue Economic Zone, specially engaging in development, production and sales of polysaccharide products. The compan...
Dongying Tiandong Pharmaceutical Co.,ltd founded in 1992, subordinated to Shandong Haike Chemical Group, is located in Dongying city, the center area of Yellow River Delta High-efficiency Ecological Economic Zone and Shandong Peninsula Blue Economic Zone, specially engaging in development, production and sales of polysaccharide products. The company is entitled as High and New Tech Enterprise in ShandongProvince. The company focuses on low-molecular weight heparins, heparin sodium and heparin calcium and so on, as the biggest low-molecular weight heparin API manufacturer in China. The injection workshop has been built with annual capacity of 21 million units of aqueous solution injections, which makes the company to have the complete industry chain from API to injection product and updates the heparin industry chain. Tiandong company is the only one to pass EDQM inspection, granted COS for enoxapairn sodium in China. Moreover, its enoxaparin sodium has been granted with Brazil GMP certificate, Swedish GMP certificate and French GMP certificate successively, and completed the registrations in many other countries and regions, and has been exported to more than forty countries in the world. The company keeps long-term close partnership with School of Pharmaceutical Sciences, ShandongUniversity, which strengthens our innovative ability of R & D. The company has applied 15 invention patents or utility model patents associated with heparin products. In 2009, the company has undertaken the national Major Creation of new drugs project on Quality Standards Study and Establishment of Five Low Molecular Weight Heparins. Over 20 years, the company has always made efforts to provide better pharmaceutical products and services for people, and established impeccable production service management system and quality management system by years of practices and innovation to assure product quality and the interests of clients.

01

Dalteparin sodium

China

Antibody Engineering

Not Confirmed

Dalteparin sodium

China

Antibody Engineering

Not Confirmed

Dongying Tiandong Pharmaceutical Co., Ltd.

About the Company : Dongying Tiandong Pharmaceutical Co.,ltd founded in 1992, subordinated to Shandong Haike Chemical Group, is located in Dongying city, the center area of Yellow River Delta High-efficiency Ecolog...

Product
Web Link

Stock Recap
#Pipeline Prospector

Market
Place

Only 10 entries up to this point, click to access all

FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]

Inspections and registrations

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FDA

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EDQM

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ABOUT THIS PAGE

Contact Dongying Tiandong Pharmaceutical Co., Ltd. and get a quotation

Dongying Tiandong Pharmaceutical Co., Ltd. is a supplier offers 3 products (APIs, Excipients or Intermediates).

Find a price of Enoxaparin Sodium bulk with DMF, CEP offered by Dongying Tiandong Pharmaceutical Co., Ltd.

Find a price of Heparin Sodium bulk with DMF offered by Dongying Tiandong Pharmaceutical Co., Ltd.

Find a price of Dalteparin sodium bulk offered by Dongying Tiandong Pharmaceutical Co., Ltd.

Company profile for Dongying Tiandong Pharmaceutical Co., Ltd.

VISIT THE VIRTUAL BOOTH

Review portfolio & marketing content

CONTACT DETAILS

Google Map, LinkedIn, Emails...

EVENTS

Webinars & Exhibitions

DIGITAL CONTENT

INTERVIEW #SpeakPharma

VLOG #PharmaReel

DATA COMPILATION #PharmaFlow

4 NEWS #PharmaBuzz

ACTIVE PHARMA INGREDIENTS

3 All APIs

3 USDMF

1 CEP/COS

2 KDMF

2 NDC API

1 Listed APIs

INSPECTIONS & REGISTRATIONS

1 FDA

2 EDQM

01

02

03

JDW Pharmaceutical Co., Ltd.

2019-11-20

20160509-124-G-129-05(1)

Dongying Tiandong Pharm. ...

China

No.1236, Nan-er Road, Don...

01

Samoh Pharmaceutical Co., Ltd.

2016-05-09

20160509-124-G-129-05

Dongying Tiandong Pharm. ...

China

No.1236, Nan-er Road, Don...

02

01

02

01

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