MmS   Medimar Solutions


Services to Sites

Assistance in starting new Sites

If you are interested in opening a new research site, we offer assistance on site requirements, interview and selection of personnel, training on GCP and FDA regulations (see the trainings we offer)

Assistance in starting new studies

We provide assistance during the preparation of new studies. This includes the preparation of regulatory documents, assistance in training and access to the supplier portal, and preparation of original study documents.


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QA

We offer Quality Control during studies with periodic visits to the site to review:

• Regulatory Documents for the completeness and accuracy of essential documents

• Review of original documents to ensure they comply with ALCOA standards.

• Review of study drugs for reconciliation and accounting.

• Any other site requirement according to the contracted services.

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Provide Research Studies

We assist sites in obtainingeitherno of new clinical studies according to the experience and performance of the site

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