eChinaChem, Inc., the China subsidiary of Pacific Genuity, Inc. (San Carlos, California), provides an integrated...
Lychee Group is a media company specializing in China's life sciences industry. Through our targeted events, we bring together the business leaders that are shaping the fastest growing life sciences market ...
Key Capabilities for Chinese clients: -Regulatory affairs -Assembly of common technical documents / biologics license applications -Advice & assistance for development and scale-up -Assistance ...
--
1.Facilitator for western customers to access China 2.Bridging the gaps of the cultures and distances 3.Supplier evaluation and technical support 4.Quality system implementation
Many of our major customers have elected to run teams of scientists (or Full-Time Equivalents) at WuXi PharmaTech. This "FTE-based" approach to working with WuXi PharmaTech enables our customers to submit ...
Accelovance (China) operates to deliver ICH-GCP compliant clinical trials. Its staff has strong experience in conducting ICH-GCP clinical trials for multinational client and it utilizes the same clinical ...
Outside of China, Vivo Development Ltd has now established a partnership with Arianne (www.arianne-consulting.com). Arianne Consulting is a Clinical Contract Research Organization headquartered in the ...
Tigermed Consulting Corporation Translation Department is a professional translation team especially in medical sciences. It owns more than 10 full-time translators and approximately 20 part-time translators; ...
The Process Group at ChemPartner provides contract R&D and manufacturing services to clients by developing cost efficient and environmentally benign processes for bulk chemical production. The process ...
We provide the following service: Medical Translation Pls contact with us.
We provide the following service: Training on Clinical Psychology Pls contact with us.
We provide the following service: MKT Strategy & MKT Research Pls contact with us.
Contents 1. Protocol and Case Report Form(CRF) design 2. Clinical rerearch center evaluation 3. Item management 4. Clinical trails monitoring(international multi-center clinical trails, import registration ...
The European Union Clinical Trials Directive's primary purpose is to establish a legal basis for adherence to Good Clinical Practice (GCP) guidelines in the conduct of human clinical trials throughout ...
1. National and international regulatory strategy and development for the biopharmaceutical, medical device, veterinary and biologics industries 2. Regulatory submission (IND, CTA, NDA, CTD, eCTD, DMF, ...