03345033948 | swapan@infoclinconsultancy.com

What We Offer

Infoclin LLP provides a robust suite of services designed to support pharmaceutical companies, CROs, and medical institutions in navigating the complexities of clinical trials.

1. Clinical Trials Department Establishment & Management

End-to-end support for setting up and managing clinical trial departments within medical institutions...

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2. Overall Execution of Study On-Site

Comprehensive on-site study management and execution, including patient recruitment strategies, data collection...

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3. Conduction of GCP Training Workshops

Regularly conducted GCP (Good Clinical Practice) training workshops to ensure all research personnel are up-to-date...

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4. Audit Support & Quality Control Services

Providing robust audit support and quality control services to ensure all clinical trial activities comply...

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5. Ethics Committee Registration & Re-Registration

Comprehensive guidance and facilitation for Ethics Committee (EC) registration and re-registration processes...

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6. Medical and Regulatory Writing & Publications

Expert medical and regulatory writing services for clinical study protocols, reports, and scientific publications...

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7. Providing Qualified & Skilled Manpower

Offering access to a pool of highly qualified and GCP-trained professionals, including Clinical Research Coordinators...

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8. Regulatory Affairs & Proceedings Handling

Expert navigation through complex regulatory landscapes, including submission management, liaison with authorities...

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9. Archival of Clinical Data

Secure and compliant archival solutions for all clinical study data, essential documents, and regulatory submissions...

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Patient Recruitment and Retention

Supporting seamless patient recruitment and retention through ethical outreach, education, and clear communication...

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Why Choose Infoclin LLP?

Our Commitment to Excellence

Unwavering Dedication to Quality and Ethics

Choosing Infoclin LLP means partnering with a team that prioritizes scientific integrity, ethical conduct, and patient safety above all else. Our deep understanding of the Indian clinical trial landscape, combined with our global expertise, allows us to deliver results that are both compliant and impactful.

  • Experienced Team: Highly skilled professionals with extensive industry knowledge.
  • Tailored Solutions: Customized strategies to meet the unique needs of each trial.
  • Regulatory Acumen: Navigating complex regulations with ease and precision.
  • Patient-Centric Approach: Ensuring the well-being and rights of participants.
  • Proven Track Record: A history of successful trial management and positive outcomes.