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    MedClinica is a Scientifically - Driven CRO, delivering strategic solutions in providing comprehensive Clinical Research Services for Pharmaceuticals, Biologics, Medical Devices, Nutraceuticals & Ayurveda companies.

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    MedClinica recognizes that Quality is an integral part of its operations, & it is the primary responsibility of each and every employee. This is the key to a healthy business.

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    MedClinica delivers exceptional & customer-success-enabled services with top-notch quality supported by flexible timeframes & cost-effectiveness.

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    MedClinica delivers projects in strict adherence to ICH-Guidelines and applicable regulations i.e.. EMA, US FDA, & DCGI, and also in compliance with the protocol, and other statutory legal requirements.

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    MedClinica’s team is comprised of pharmacy and medical industry experts. The team is a perfect blend of rich experienced professional graduates and postgraduates - MBBS, MD, Pharmacy & Life Sciences.

ABOUT US

MedClinica was founded with a vision to support the Pharmaceutical, Biologics, Medical Device, Nutraceutical, and Ayurveda industry. To manage comprehensive Clinical Research Services through the compliance process, and in strict adherence to ICH Guidelines, and applicable regulations i.e.. EMA, US FDA, & DCGI, Protocol, & other statutory legal requirements.
MedClinica team is expertise, competitive cost, and uncompromised quality within the committed timelines.
MedClinica’s team is comprised of pharmacy and medical industry experts. It is a perfect blend of rich experienced professional graduates and postgraduates-, MBBS, MD, Pharmacy & Life Sciences
MedClinica deliver’s exceptional and customer-success enabled services with top-notch quality, supported by flexible timeframes & cost-effectiveness. MedClinica works diligently to be trustworthy & forge a Strategic Partnership with our customers.
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Drug Regulatory & Medical Writing

Medclinica providing regulatory services to all Pharmaceuticals, API manufactures and Biotech companies

Clinical Trial Management

Experience in conducting end to end multicentre global trails in all therapeutics areas.

Clinical Data Management & Biostatistics

Experience in end to end Clinical data management, Biostatistics & Programming inclusive of CDISC(SDTM&ADAM) &CDISC (SEND) & AI

Safety and Pharmacovigilance

Experience in safety reporting for all phases and Post marketing surveillance

Medical Devices

Experiencing in managing all types of global medical devices end to end clinical trial services.

Quality & Audit Services

Teams with skills of ICH-GCP, US FDA, EMA and all other regulatory

OUR SERVICES

Medical & Scientific Writing

We offers :-
  • Medical Writing
  • Clinical Operations & Project Management
  • Clinical Data Management
  • Biostatistics & SAS Programming
  • Regulatory Consulting
  • Quality & Audit Services
  • Safety & Pharmacovigilance
  • Medical Device
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News & Events

Publish What You Think

Read & get educated & knowledge over versatile laboratory technology.We how else you can help patients without being a doctor.
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Admin Mar 15 2022
Do You Want To Fast Track your Lab Operations

Given the extremely competitive environment; we understand the situation of pathologists and lab owners. So, fast track your operation.

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Admin Mar 15 2022
Learn: Blood bank operations and management

Blood bank inventory management in India We study the current blood-banking scenario. Identify challenges that are peculiar to banks.

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Admin Mar 15 2022
Equipping Researchers Lab in the Developing.

Clinical laboratory tests are taken up for the diagnosis, prevention and treatment of diseases and the branch of healthcare deals.

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