At G&L Scientific Inc., we believe that every project is unique. Hence, we offer a flexible approach to meet our clients’ specific needs. We work closely with companies to develop and maintain sustainable GMP and GCP complaint programs and quality systems.
GMP applies to all drug development steps from pre-clinical to commercial products and requires the use of systems, starting materials, active substances, equipment and facilities that meet specific standards and requirements.
Poor quality products pose unnecessary risks to patients and consumers and will result into a waste of time, effort and resources as these products cannot deliver the intended treatment results and therapeutic effect.

  • Site and/or System Gap Assessment
  • Hosting and/or Assistance of Regulatory Authority Inspections
  • Oversight of suppliers
  • For cause audits
  • Assessment, development and implementation of GMP Quality system
  • On-site and/or remote Quality support
  • Remediation
  • Person in Plant
  • Support application, amendment and renewal of Drug Establishment Licence
  • GMP training
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