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Part of US based
Semler Group of Companies,
in business since 1946

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Service Overview 2

"What we do for customers is create an instinctive GxP expertise in their employees - where quality comes as naturally as driving a car. Unlike other consultancy firms, SRC does not just identify gaps in process, we proactively engage with our clients to fill them through rigorous and customized training and handholding.” - Dr. Krathish Bopanna, President & Chief Executive Officer

The dynamic world of the bio-pharmaceutical industry is characterized by perpetual change. Semler Research Center's 20+, full-time professionals offer constant, consistent and science-driven expertise that help pharmaceutical, biotech, medical, manufacturing, engineering and technical writing industries achieve their goals in the ever-increasing regulatory environment for obtaining regulatory approvals, improving their efficiency and reducing costs and operational deviations. Whether the projects are in engineering, consulting or management, our energies are constantly directed at fulfilling our customers' expectations on time and on solid commercials. We facilitate certifications that are valid and recognized across continents - North America, Europe, South Africa, South America and the Asia Pacific region.

We offer a complete range and depth of services that include quality management systems, GxP audits, gap analysis, facility up-gradation, training and development, skill development and assessment, dossier preparation and submission, international regulatory audit support and qualification & validation of systems and processes.

We serve:

  • Virtual pharmaceutical companies
  • Manufacturers of active substances (API)
  • Manufacturers of medicinal products (sterile & non-sterile)
  • Manufacturers of medical devices
  • Suppliers and contractors to registered manufacturers
  • Manufacturers of OTC medicinal products
  • Companies importing to regulated markets