MAXIMA Health Research can provide service and act as a consulting agent in the field of regulatory support in all CIS countries.

  • Completion of documents, required for product registration
  • Collecting and handling the dossier for the primary registration/renewal/inclusion of changes according to the legislative requirements
  • Support of all the stages and procesess of registration in the local agencies and authorities
  • Development, approval and implementation of various types of packaging and local labeling in the manufacturing process
  • Applications to patent authority, support for patent protection and protection of trade names at the different stages


MAXIMA could provide service and act as your consulting agent in all CIS countries.

Quality assurance system and GMP compliance

Quality Assurance require participation and responsibility from all departments of the company at all levels, as well as suppliers and distributors. When all participants of the pharmaceutical market has to learn new methods of management and quality assurance "on the job", our company offers:

  • system of standard operating procedures (SOPs) and their modernization;
  • risk analysis of the existing system of quality;
  • preparations for the audits;
  • training programs for staff.

If you are interested in our service
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