Neopharm is committed to providing its clients with the highest quality in analytical (chemistry, chromatography, microbiology), consulting, stability, development and validation services. We strive to respect client timelines, as well as the accuracy and integrity of all data generated while performing tests or projects. We pride ourselves in ensuring our facilities, equipments, records and procedures are maintained in accordance with applicable regulatory and compendial requirements with respect to the Client's specifications.
All analyses are performed in compliance with cGMP requirements using methods in accordance with compendial procedures including but not limited to: USP/NF, BP, Ph. Eur, JP, CP, FCC, ACS, AOAC, AOCS, AAMI, AWWA, FDA-BAM, In-house and client supplied methods.Over the years, Neopharm has successfully developed/validated/transferred in excess of 3,000 HPLC, GC or other chemistry analytical procedures.
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