Clinical studies are crucial to the process of bringing a new medical product to the market.  Conducting a clinical trial in an ethical and appropriate manner is a key factor in ensuring a successful regulatory submission and later, the sales process.  

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With a combine forces with GNA Research Ltd, HaMaDa can provide a unique opportunity to deliver a clinical research program with the best possible results and excellent performance.  As a full-service clinical research partner, we will take care of the Design, Management and Execution of your Clinical Study. Services available include:

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Clinical Trial Preparation

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• Clinical trial design and development

• Protocol development

• Site selection and qualification

• Initial Regulatory Submission

• Investigator meeting planning, production, and execution

• Establishment of Electronic data management trough EDC partners

• Preparation of clinical submission documents

 

Clinical Trial Conduct

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• Ongoing Regulatory submissions

• Study management

• Site monitoring visits (on-site and remote)

 

Additional Clinical Services

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• Overall Clinical Development Strategy

• Combination of Clinical, Regulatory and Publishing strategies

• Publishing of Scientific abstracts and articles

• Clinical Study reports (CERs, Final CSRs)

• Medical Writing

• Literature Search

• GCP audit

• Trainings to company's staff on clinical research and medical writing topics   

• Access to nationally and internationally recognized Key Opinion Leaders (KOLs)