CRO Services

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.  

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:

Clinical Trial Preparation

  • 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

  • Ongoing Regulatory submissions

  • Study management

  • Site monitoring visits (on-site and remote)

 

Additional Clinical Services

  • 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)

Regulatory, Clinical & Quality Affairs for the MedTech Industry

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