CRO - CRRC

Contract Research Organisations in Mauritius

Contract Research Organisations (CROs) in Mauritius conduct clinical trials within their premises with the latest state-of-the-art medical equipment and comfortable facilities. Their team comprises highly qualified and experienced doctors, pharmacists, clinical research managers biostatisticians and data managers with extensive scientific expertise. Mauritius is home to internationally renown CROs, which have helped to further develop the Clinical Research ecosystem.

CROs in Mauritius conduct clinical trials within their premises with the latest state-of-the-art medical equipment and comfortable facilities. Their team comprises highly qualified and experienced doctors, pharmacists, clinical research managers biostatisticians and data managers with extensive scientific expertise. Mauritius is home to internationally renown CROs, which have helped to further develop the Clinical Research ecosystem.

List of registered CROs in Mauritius are as follows:

Procedures

Requirements for Registering as a CRO

Step 01

It is mandatory for the CRO to be registered with the council

Step 02

A CRO seeking registration with the Council shall make an application at least 2 months before beginning of operations.

Step 03

Application form and the following supporting documents should be submitted: List of supporting documents to be provided – after confirming with CRRC

Step 04

The CRO shall ensure that trials are adequately monitored.

Step 05

The CRO shall implement quality assurance and quality control as per standard operating procedures designed for the purpose. Application for a clinical trial licence – to be put in the form of a flow chart by Communications team

Step 06

Write a formal application addressed to the CRRC requesting the medical trial license

Step 07

Prepare the required supporting documents

Step 08

Submit application with all the required documents and fees to the CRRC for verification. The application fee per trial is at MUR 10,000

Step 09

Board of the CRRC will assess application and confirm if all the required documents are provided.

Step 10

Upon the assessment process, the CRRC can request for additional documents

Step 11

If application is complete as required by the CRRC, then CRRC will forward the application and the documents to the Ethics Committee (EC) for approval.

Step 12

The EC will review the application and the provided documents then they will decide to approve or reject the application.

Step 13

After the review by the EC, the CRRC will inform you of the application decision

Step 14

If application is approved by the EC and the CRRC, licence fee is paid

Step 15

Issuance of clinical trial licence, subject to a payment of a licence fee of MUR 100,000

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