Regulamedica

Regulamedica is seen to be a one-stop location in order to obtain regulatory information as required in medical device development, market authorization, distribution and related processes.

The Regulamedica Guidelines identify national regulation and summarize on registration steps, documentation assembly, content of application forms, labeling requirements, review timeline, submission rejection remedies, pricing and more details in order to register medical devices at national responsible agency.
Regulamedica Guidelines summarize requirements overview in the following areas:
– Medical device registrations,
– Establishment registrations,
– Clinical affairs;

Where you should experience the following benefits as provided by Regulamedica:

Information instantly available at your fingertips
Avoid time consuming process of investigating regulatory requirements,
Save resources and learning hassle,
Supported by Regulamedica professionals for any open Question
Lesson learned, etc…

Development of new guidelines and updates of existing ones is an ongoing process at Regulamedica, therefore we would very much appreciate your feedback on purchased material.
For more details, questions and purchase of the Regulamedica Guidelines, please dot hesitate to contact us. We offer free samples for your orientation.

Company’s Keywords:

regulatory requirements, market approvals, medical devices registration, wholesaler registrations, manufacturer registration, clinical trial registration