+1-289-642-2696   |   info@krinslifescienceslab.ca

Consultancy Services

With several years of experience in the life sciences industry, our team understands the importance of general manufacturing practices (GMP). Our team can help you to solve an array of issues related to manufacturing practices, process validations, our professionals advise companies according to industry standards and regulations. Our quality assurance and regulatory consultants offer necessary support demanded by companies. Providing assistance to a wide array of FDA regulated industries, including pharmaceuticals and nutraceuticals, our service helps manufacturers, importers, and packagers attain site licenses in Canada and the United States.

Our Service Portfolio Includes:

  • cGMP Assessment of Production Facilities
  • Third Party Audits of Suppliers and Contract Manufacturers
  • Review and Preparation of Quality Agreements
  • GMP Staff Training
  • Quality Control Testing Review
  • Document Design
  • Document Preparation
  • Corrective and Preventative Action
  • Quality Control and Quality Assurance
  • Addressing GMP Audit Observations