cGMP LABORATORY SERVICES

The pharmaceutical testing laboratory has been evolving constantly to offer innovative services. While it is imperative for manufacturers to implement current Good Manufacturing Practices (cGMP), it is essential that GMP and GLP analytical packages extend support throughout the entire life cycle from early phase of drug development, to regulatory submission, GMP manufacturing and drug released post marketing analytical testing requirements.

At UMED, we offer a comprehensive range of highly specialized testing services using advanced technologies. We adopt a flexible service approach and our service design is in accordance with the customer’s requirements to meet 21CFR

We are familiar in providing various activities by using advanced sophisticated instrumentswith multiple technologies. We are pleased to invest for meeting quality compliances with scientific justifications by following current guidelines and regulatory requirements which is achieved by multi-disciplinary team.

UMED is involved in facilitating regulatory driven services such as Method development, Method Validations, Elemental Impurities, Extractable and Leachable and Physical characterization, Stability Studies by different techniques such as HPLC, GC, GCMS, LCMS, PSD, ICPMS and X-RD etc.

Well experienced in handling thousands of projects of varied scope and complexity for Domestic to MNC’S organizations. We are equipped to deliver even the most complex critical projects with ease. For a detailed overview on our scope of services,

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