Techpool Bio-pharma Co., Ltd. Company Profile
Established in 1993, Techpool Bio-Pharma Co., Ltd. is one of the leading bio-pharma companys in China, with total assets of USD30 million and registered capital of USD11.7 million. We are specializing in R&D, manufacturing and marketing of bio-pharmaceutical products and currently export to Japan, Korea, India, Pakistan, Israel etc.
We manufacture the following pharmaceutical products:
Finished products
1. Ulinastatin for Injection
2. Human Chorionic Gonadotropin for Injection
3. Urokinase for Injection
4. Human Urinary Kallidinogenase for Injection
APIs
1. Urinary Trypsin Inhibitor (UTI)
2. Human Chorionic Gonadotropin (HCG)
3. Human Menopausal Gonadotropin (HMG)
4. Follicle Stimulating Hormone (FSH)
5. Urokinase (UK)
Location
89 Gaopu Road, Gaotang Scien-tech Industrial Park, Tianhe, Guangzhou 510520, P.R.of China
Guangzhou
Guangdong
510520
China
Contact
Phone: +86-20-87037288
Fax: +86-20-87037999
Email: yuxp@techpool.com.cn
News Articles
Techpool In-Licenses China Rights to Bone Cancer Drug from Roche
Guangzhou Techpool Bio-Pharma in-licensed the China rights to Bondronat, an oncology drug from Roche. Bondronat is a treatment for metastatic bone cancer. It treats pain along with fractures, spine co...
Roche and Takeda’s Techpool to maximize Bondronat in China
Roche has signed a contract with Takeda subsidiary Techpool Bio that will allow the Chinese pharma company exclusively to market the Swiss firm's oral bisphosphonate drug for bone metastases Bondrona...
Roche Grants First Drug License In China, To Takeda-Owned Drug Maker
For the first time, Roche has licensed one of its drugs, Boniva (ibandronate), a chemotherapy drug for treating cancer cells, to a China-based company, albeit it Techpool Bio-Pharma.
Roche Grants First Drug License In China To Takeda-Owned Drug Maker
For the first time, Roche has licensed one of its drugs, Boniva (ibandronate), to a China-based company, Techpool Bio-Pharma, which is owned by Takeda.
Week in Review: WuXi PharmaTech and PRA Form Clinical CRO JV
WuXi PharmaTech is forming a JV with PRA, a US-based clinical-stage CRO, that will offer Phase I-IV clinical trial services in China; ShangPharma agreed to a go-private offer from its Founder and TPG...
Pharma 3.0 Pulls Companies into the Digital Future
Social media and mobile marketing have kick-started the pharma industry into a phase dubbed Pharma 3.0. Gone are the days of Pharma 1.0 in which companies could rely on a handful of blockbuster drug...
Big pharma companies BMS and Merck are pharma partnering on Daclatasvir
Big pharma company, Bristol-Myers Squibb, is pharma partnering with another big pharma company, Merck, to develop Daclatasvir to treat Hepatitis C. The big pharma companies will work on the hepatitis...
Merck enter pharma partnering pact with Ra Pharma for cyclomimetics
Ra Pharmaceuticals has entered into a pharma partnering deal with Merck, a top 50 big pharma corporation, focused on the development of Cyclomimetics, a new class of compounds that have the diversity...
Drugs and Medications
Fluoride [Libertas Pharma, Inc.]
Fluoride Chewable Tablets 0.5 mg
Fluoride [Libertas Pharma, Inc.]
Fluoride Chewable Tablets 1 mg
Metoprolol tartrate [Med-Health Pharma, LLC]
Metoprolol Tartrate Tablets, USP
Rx Only 45% Urea Nail Gel In a vehicle containing Camphor, Eucalyptus Oil and Menthol )
PubMed Articles
Structures containing the (R)-3-amino-3-methyl piperidine unit as a new pharmacophore moiety have been shown to possess moderate inhibitory activity for DPP-4 with good pharmacokinetics profile. One o...
Is pharma running out of brainy ideas?
Clinical Trials
To demonstrate the relative bioavailability of Sandoz Inc. and UCB Pharma, Inc (Keppra) 750 mg Levetiracetam tablets in healthy adult volunteers under fasting conditions.
Pharma-Pen (Formerly Innoject) Auto-Injectory TIV
The purpose of this study is to evaluate the safety, effectiveness, and tolerability, of the Pharma-Pen(TM) intramuscular (IM) and subcutaneous (SC) auto-injector systems used by untrained...
To Demonstrate the Relative Bioavailability of Cilostazol 50 mg Tablets Under Fasting Conditions
To demonstrate the relative bioavailability of Cilostazol 50 mg tablets under fasting conditions.
This is 2-armed parallel group, prospective, randomized, open-label, multicenter Phase 3 controlled trial to establish the efficacy and safety of conversion from maintenance immunosuppress...
Development of a New Method for Analgesia
Aim: To examine a new method to perform local anesthesia in order to diminish the inconvenience by the procedure in patients before performing intubation or oesophagogastroduodenoscopy.
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