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Lab Testing Equipment

Clinical Trial Services

VaidyaRx supports pharmaceutical, biotechnology and clinical research organizations globally with clinical trial consultation and end-to-end clinical trial support services in India.

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We collaborate closely with each client to understand their unique needs and study goals, then guide customized trial strategies and operational plans tailored to those requirements.

Clinical Trial Consultation

  • Regulatory, CDSCO & Import Licensing Advisory

  • Gap and risk assessment in regulatory data packages

  • Quality Assurance & Audit Readiness

  • Strategic Program Planning & Review

  • Organizational Readiness for ICH E6 (R3) Compliance

  • Clinical Trial Planning & Compliance Requirements

End-to-End Clinical Trial Services

  • Development of Clinical Trial Protocols

  • Development of Standard Operating Procedures

  • Training of Human Resources involved in clinical trials

  • Preparation of the trial related documents

  • Selection of trial sites 

  • Preparation and Submission of documents for review by IRB and institutional Ethics committee

  • Identification and briefing of presenters for SEC meetings, preparation of presentation materials, and support in addressing SEC queries

  • Preparation and submission of clinical trial application along with protocol to CDSCO

  • GCP Training and compliance

  • Provide advice on safety management including medical management and compensation

  • Collection and acquisition of trial case record data, statistical analysis, and preparation of reports in consultation with the investigator

Why Choose VaidyaRx

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✔ Senior consultants with extensive industry experience

✔ Flexible and customized engagement models

✔ Cost-effective and scalable solutions

✔ Strong focus on quality, compliance, and inspection readiness

✔ Result Driven approach

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