About Us

About Clinimerck

Clinimerck Global Research Solutions LLP., established in November 2021 is a full-service capability CRO headquartered in Mumbai, India. We provide a wide range of CRO services to sponsors of the world in Clinical Trial, Site Management, Clinical Data Management, Medical Writing, and Regulatory affairs in pharmaceutical, a medical device company, biotech, ayurveda, homeopathy, and operate in India from 2 locations (Mumbai & Kerala).

We ensure that a trial moves faster through the value chain and results in shorter timeliness to get to the market, we are committed to maintaining the standards of ethics and transparency while applying the latest analytics for data management and new-age innovation in therapeutics.

How We Help

Clinimerck offers a broad range of specialized services to various industries such as pharmaceutical, biotechnology, medical device companies and national agencies to bring new drugs and devices to the market faster.
Our full range of services spans the entire lifecycle of product development and can be adapted to suit national trials or global programs. 

Why Us?

We are Multifaceted Proficients who have brought together the Medical, Pharmaceutical, and Life science sectors under One Umbrella. Our reach among Renowned Doctors, Established Pharma companies, and Innovative Scientists has succeeded in Meaningful, Applicable, and Beneficial Clinical Research Studies.
Our team is dedicated to providing Strategic Solutions for your Clinical Queries and conducting Credible studies to get Productive Results with immaculate Clinical data management. 

Benefits Available

Our focus is always on designing a package of services to meet the organization's needs and study requirements. Our ideology to customize and blend with your requirements makes us an alluring Contract Research Organization

Expanding
Our Collaborative Networks

Building strong partnerships with leading institutions to drive innovative research and development globally.

Quality Assurance

Our Quality Assurance framework is designed to ensure the highest level of compliance, ethical integrity, and research excellence, providing a robust system of internal audits, regulatory alignment, and proactive client engagement to guarantee the quality and reliability of all research activities.

  • Clearly outlined SOPs and comprehensive understanding of local regulatory requirements.
  • Conducting internal audits by our expert QA representatives to assess compliance and readiness for external audits and regulatory inspections.
  • Upholding ethical standards and ensuring that all research activities are conducted with integrity and in compliance with ethical guidelines.
  • Interacts with clients to discuss quality-related matters, address concerns, and provide assurance regarding the quality of research processes and outcomes.

OUR VALUES

Vision

Clinimerck aims to be a leading clinical research leader, focusing on medical innovation and patient outcomes. They conduct high-quality, ethical research, foster collaboration, and use cutting-edge technology to transform healthcare globally, contributing significantly to the future of medicine and patient quality of life.

Mission

At Clinimerck, our mission is to conduct rigorous and ethical clinical research that accelerates the development of safe and effective therapies. We are committed to fostering innovation, ensuring patient safety, and maintaining the highest standards of quality and integrity in all our studies. By collaborating with stakeholders and leveraging advanced technologies, we aim to deliver impactful research outcomes that improve healthcare and enhance the lives of patients globally.