BBPL is also working in the Drug development process for our International Client.
BBPL helps them to register their product in India by conducting the efficacy and safety Clinical Trial.
BBPL does all the process of conducting the Clinical Trial. (Clinical Trials Management, Clinical Site Monitoring, Audit, Data Management, Medical Writing, SOP writing, Pharmacovigilance, BA/BE and pilot BA/BE study).
BBPL has great collaboration with various esteemed Government and Private Hospitals all over India.
BBPL also has collaboration with different Research and Analytical Centers who have global presence for providing their state of art facility services.
BBPL has good numbers of experienced and enthusiastic team members who are expertise in their respective area. BBPL provides time to time training to all centers for upgrading their knowledge about Current Regulatory Guidelines and Good Clinical Practices (ICH, Indian GCP).
BBPL does their research in strict compliance with national and international regulatory guidelines that are assured by our QA Department and also by Independent Auditors.
Major Work In Clinical Trial
Clinical trial Phase I-IV (Domestic & Global)
BA/BE & Pilot BA/BE Studies
Regulatory support for Clinical Trial
Data management
Medical Writing
Monitoring/ Auditing and SOPs writing
Pharmacovigilance
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