With experience of above 30 years we can guide to address challenges in product development - analytical method development, validation, method transfers, de-formulation (Q1,Q2 and Q3), product performance evaluation, stability studies, technology evaluations appropriate to the scope and criticality of projects, CMC support of drug substance and drug product. DMF review, regulatory queries for all markets, general laboratory operations/GMP/GLP and in the evaluation of new drug technologies formulations (orals and non-orals). Quality – compliance assessments, remediation plans, OOS/deviation policies and investigations, data integrity investigations and validation. Services can be provided in-house, on site at multiple client locations or at third party facilities. We can supply best quality API, pharmaceutical intermediates, impurities standard, chemicals and consumables as per requirement of our valued clients.
// Our Team
27/Broadway Business Hub, Opp. to Bharat Petroleum Bhayali, Vadodara-391 410, Gujarat. India.
+91 94263 32930
yuvaraj@shriharipharmachem.com
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