Ahmedabad

Accuprec Research Labs Pvt Ltd. is FDCA approved, OECD-GLP, NABL accredited and ISO 9001:2015 certified CRO. Head Quarter of the CRO is located at Ahmedabad and branch offices at Canada and USA.

Expertise in Nitrosamine and elemental impurities and recent regulatory updates. Handling of analytical instruments e.g. HPLC, UPLC, UV, KF, Particle Size, Dissolution, LCMS, GCMS, ICPMS and Zetasizer. Expertise in Analytical Method Development Assay/ RS/CU/ Dissolution and report writing.

After a journey of growth spanning 27 years as Cadila Healthcare Ltd. and the Zydus Group, we have evolved and transformed ourselves in response to the changing times.

Monitoring of analytical functions and ensuring real-time analytical support to the cross-function team to achieve the timeline of different projects. Analytical method validation of drug substance and different dosage forms.

Supervise and lead the team of analytical development, Analytical method validation, technology transfer, forced degradation study, preformulation study, dissolution studies, Extractable and Leachable and technical query handling. Candidates must have exposure of Pharma regulatory approved organisations USFDA, MHRA, Eu and other Major regulatory bodies

Lead and mentor a team of research scientists and chemists. Oversee projects, ensuring timely, budget-friendly, and high-quality delivery. Provide expertise in solving complex synthetic challenges and optimising reactions

Analytical Method Development, Validation, Transfer activities of test like Assay, RS, Dissolution and Solvent. Calibration of the Analytical instruments like HPLC, GCHS, IR, UV & Disso as per the master calibration schedule. Carry out routine analysis & Ensure documents pertaining to day to day analysis.

Reviews all Annual Product Quality Review APQR reports received from manufacturing partners and prepares APQR reports other than those received from the manufacturers within the prescribed time frame.