Sristek

Sristek is committed to be the CRO of first choice in the area of contract research services by combining extreme focus on quality and compliance to regulations & guidelines with operational excellence and continually improve the effectiveness of the Quality Management System in line with the customer’s requirement.
For vacancies at Sristek.........click here.

CLINICAL AND POST MARKETING SAFETY

The EU Clinical Trials Directive has provided Europe with its most comprehensive revision of clinical trial process. At the heart of this revision was expedited (including electronic) and annual safety reporting. Furthermore, post-marketing surveillance in the new 27 Member State Europe has never been more detailed. Electronic safety reporting, new pharmacovigilance inspections, the role of the Qualified Person for pharmacovigilance, licensing agreements and safety data exchange, and the revised Volume IXa are all new challenges that face multi-national companies.This course provides pharmacovigilance personnel with the tools to remain compliant, and the knowledge of what needs to be reported when and to whom........read more..............

Sipra Labs Pvt Ltd

SIPRA LABS is USFDA registered and DSIR approved Contract Research Organization engaged in Drug Development support services to the Pharma Industry. The Centre has a team of 150 scientists engaged in different innovative Research Projects for global regulatory submissions. The thrust of the Organization is to create one-stop-research solutions to the Drug and Pharmaceuticals Industry. SIPRA, a dedicated research organization, collaborates with the industry in conducting the studies as per GLP / GCP guidelines. SIPRA is preferred research organization for the clients across the globe.
For vacancies at Sipra Labs Pvt Ltd .........click here.

Synchron  is a leading contract research organization in India, designed to meet the specific requirements of the clients in the field of clinical registration of new pharmaceutical products and medical devices, from phase I to phase IV, including Bioequivalence, Bioavailability, Pharmacokinetic/Pharmacodynamic studies, Statistical Analysis and Data Management strictly adhering to ICH and GCP guidelines. The company offers competitive and high quality clinical trial services to domestic and international pharmaceutical and Bio-Pharmaceutical companies.......




For Career with us click here