Medical Regulations Services
is a consulting office, located in the capital of Canada to serve the
comprised of a diverse group of scientists with unique understanding of
Canada, USA, and other foreign countries food and drug regulations.
Our highly qualified consultants
have established a superior reputation for their work quality, expertise, and
can offer clients complete turnkey solutions that includes:
QMRS prepares, compile, and submit product registration packages
(Generic drugs, Cosmetic, NHPs, Novel food etc.) as per Health Canada
SITE (ESTABLISHMENT) LICENSING
QMRS conducts “Third Party Audit” to assess the degree
to which the facility is fulfilling the
applicable GMPs requirements.
We provide a "Certificate of GMP Compliance”,
if the facility found to be fulfilling the GMP requirements.
GOOD DOCUMENTATION PRACTICES (GDPs)
QMRS provides assistance to establish the needed SOPs and all other documentation requirements pertaining to GMPs and Good Clinical Practices.
Our documents are written according to the FDA, Health Canada, ICH, and WHO Guidelines.
CRITICAL CONTROL POINT (HACCP)
adequacy of the facility prerequisite programs
and design & develop the format of successful HACCP plans.
QMRS issue a “Certificate of HACCP Compliance”, if the facility found to be fulfilling the HACCP
GMP & HACCP
QMRS provides GMP training on drug, dietary supplements and
NHPs regulations. Also, on Good Documentation Practices, and HACCP.
We issue many types of certificates that needed
by regulatory authorities. QMRS HACCP Training Courses are accredited by the
“International HACCP Alliance”. Please
Privacy and Liability
196 Annapolis Circle,
Ottawa; Ontario K1V 1Z1 CANADA
email@example.com, Telephone: 613-526 0471, Fax: 613-526