추가 설명:
Neopharm's chemistry team tests raw materials, finished products, and packaging components against compendial methods including USP/NF, BP, Ph. Eur., JP, CP, FCC, ACS, and AOAC/AOCS, as well as in-house and client-supplied procedures, having developed, validated, or transferred more than 3,000 HPLC, GC, and other analytical methods over the years. Testing covers pharmaceutical, veterinary, cosmetic, antibiotic, enzyme, and natural health products, plus finished goods, raw materials, container and packaging components, in-process materials, utility systems, and gel capsule analysis meeting current USP gel-strength requirements, with support extending to routine and specialized techniques for regulatory submissions such as NDA, IND, and CTA filings.
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