Tuliphall CliniResearch Private Limited is a clinical research organization company, currently operating from Kolkata, West Bengal, India. This company is focused on providing clinical research services to the pharmaceutical, biotechnology and medical device industries globally. Their services include clinical trial management, medical writing, regulatory affairs, pharmacovigilance and data management. Tuliphall CliniResearch has a team of experienced professionals who ensure quality and timely delivery of services to their clients.

Our vision is to follow strict ethical standards and guidelines to ensure the safety and well-being of study participants in clinical trials.

Tuliphall CliniResearch is committed to providing innovative solutions to meet the evolving needs of the life sciences industry. Our vision is to provide cost-effective solutions without compromising on quality. 

We are dedicated to ensuring that each clinical trial is executed to the highest possible standards. 

Our core competencies are in following areas:-

  • Product Registration support,
  • Trial Design,
  • Site Selection,
  • Project/Site Management,
  • Medical and Site Monitoring,
  • Data Management,
  • Biostatistical Analysis,
  • Pharmacovigilance,
  • Medical Writing,
  • Clinical Quality Development
  • Full Clinical Trial Management
  • Consultation Services
POST GRADUATE DIPLOMA IN CLINICAL RESEARCH

POST GRADUATE DIPLOMA IN CLINICAL RESEARCH

This course is designed towards more practical sessions for 3 months (480 hours cover 48 credits) than classroom sessions for 6 months (120 hours covers 12 credits). For further details please contact +91-9511954171/+918655074029

CLINICAL TRIALS

CLINICAL TRIALS

Please find the ongoing and upcoming clinical trials details

SITE MANAGEMENT

SITE MANAGEMENT

A thorough feasibility and site selection is the basis of any successful clinical trial

ACADEMIC TRIALS

ACADEMIC TRIALS

Capable of identifying the best investigative sites to conduct a clinical trial.

BIOSTAT IN CLINICAL TRIALS

BIOSTAT IN CLINICAL TRIALS

Our mission is to help our clients improve their clinical trial outcomes by providing expert statistical support and training services

Eminent Members in Clinical Research

Dr Amlan Kanti Sarkar, PhD in Pharmacy from Jadavpur University, Kolkata
Dr Atanu Bhattacharjee (Statistician / Epidemiologist)

Core Features

What you will get from TCR

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How We Works

Our Working Process

High-quality and innovative approaches and methodologies in Clinical Research and clinical data management, to improve the quality standard which meets the growing demand of high quality data for regulatory dossier submission by the sponsored Pharma and Healthcare industries

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Ongoing Trials

Medical Device Regulations in India

Know How

The fact that India relies on medical device imports (approximately 75–80% of revenues are produced by imported medical devices) to supply its healthcare system shows that international corporations now control the medical device business in India.

Since April 1, 2020, all medical devices must be registered under the 1940 Drugs and Cosmetics Act in order to maintain their status as one of the 23 previously notified medical devices. All Class A and B medical devices must have import licenses before being imported as of October 1, 2022. By October 1, 2023, all Class C and D gadgets that haven’t already been notified must obtain import licenses. Even though import licenses are not currently necessary for medical equipment, owners must nonetheless register their product(s) through an ePortal within a few days.

Tuliphall CliniResearch Private Limited

Kolkata Office:

Flat-401, Block-E474, Shapoorji Pallonji Shukhobrishti Housing Complex, Shapoorji, Action Area-III, Newtown, West Bengal-700135

Contact: +91-8655074029/9511954171

Email: info@tcrpl.com/dramlan@tcrpl.com/dramlankantisarkar@gmail.com

Registered Office:

Plot No. 3158, Chhatguriahati, Netaji Square Bye Lane, Cooch Behar New Town, Cooch Behar-736101, West Bengal, Ind