Your Trusted Partner For Clinical Research and Pharmacovigilance

FULL SERVICE CRO CLINICAL TRIALS

CLINEXEL is a Contract Research organization providing end-to-end services in Clinical Development, Clinical operations, medical writing, and Pharmacovigilance. Our clients include Pharma, Biotech, and Medical Device companies based in India, Europe, the US, Canada, Israel, and Singapore.

ABOUT CLINEXEL

CLINEXEL is a Clinical Research Organization providing end to end services for Clinical Research, Pharmacovigilance and Medical writing. Our clients include pharma, biotech and medical device companies based in India, Europe, US, Singapore, Israel and Canada. 

CLINEXEL is a Clinical Research Organization providing end to end services for Clinical Research, Pharmacovigilance and Medical writing. Our clients include pharma, biotech and medical device companies based in India, Europe, US, Singapore, Israel and Canada. 

CLINEXEL is a Clinical Research Organization providing end to end services for Clinical Research, Pharmacovigilance and Medical writing. Our clients include pharma, biotech and medical device companies based in India, Europe, US, Singapore, Israel and Canada.

SERVICES

CLINICAL TRIALS

CLINEXEL provides end to end services for conducting clinical trials starting from study design, feasibility studies and site selection, preparation of protocol and other essential documents, logistics and project management, clinical trial applications and approval, clinical trial monitoring, data management, statistical analysis and preparation of clinical study report.

PHARMACOVIGILANCE

CLlNEXEL is currently supporting 7 Pharma companies for Pharmacovigilance as below: End to end PV operations for US FDA and India, including case processing, periodic reports, literature monitoring, signal detection, preparation of risk management plan and evaluation of additional pharmacovigilance activities and additional risk minimization measures.

GLOBAL CLINIC DEVELOPMENT

CLINEXEL supports companies by- • Development of efficient clinical development plans acceptable to different regulatory authorities • Facilitating pre-IND, End of Phase and pre-NDA submission meetings with regulators to develop and fine tune clinical development plan • Filing and maintaining IND in US, clinical trial applications in EU and India • Global solutions for CLINEXEL clients through world-wide clinical trials.

REGULATORY AFFAIRS

At CLINEXEL, we are providing global clinic-regulatory services to companies for the development of their new chemical entities and biologicals. We have supported companies for pre-IND and scientific advice meetings for firming up their clinical development plans and regulatory strategies. We are also working on subsequent IND projects for Life Cycle Management of pharmaceuticals.

MEDICAL DEVICES

Preparation of Protocols, Informed Consent Forms, and Investigators’ Brochure • Preparation of Clinical Study Reports • Authoring Clinical Evaluation Reports including literature search protocol, PICO analysis • Post Marketing Clinical Follow-up Plans.

PHARMACOKINETIC STUDIES

CLINEXEL Team members have extensive experience in Pharmacokinetic studies in healthy volunteers and patients. Cumulative experience of the team spans ~800 studies for various markets, including PK studies in healthy volunteers, patients for Long Acting Injectables, biosimilars and inhalation products.

WHY CHOOSE US?

Senior Management With Technical Expertise And Experience

  • CLINEXEL Senior Management have worked in leadership positions in core Pharma, therefore, they have Strong understanding of the drug development processes from start to finish, and the relevant global regulatory requirements 
  • CLINEXEL core team is well versed with regulatory requirements, GCP, and GVP and applicable regulations. 
  • Regular Training by Senior team members ensures that all team members are regularly trained for all new and revised regulations and guidelines.

One Top Solution

  • We provide end to end services and cover the full array of Clinical Research and Pharmacovigilance activities 
  • Safety database, EDC systems, Local Agent, QPPV and local trial monitoring services globally provided together with our partners 
  • We have pre-qualified technology partners and logistics partners

Scalable Solution

  • Experienced team leaders and Strong procedures at CLINEXEL facilitate fast and efficient scale-up 
  • Ability to rapidly scale -up including additional infrastructure, expert resources and project training 
  • Based on client requirements, WE can quickly scale-up our services by hiring additional staff as well as through process automation and cognitive automation

ISO Certified

(ISO 9001:2015:QMS)

(ISO / IEC 27001 : 2013 :ISMS)

Association of International Contract Research Organisationss

CLINEXEL Is a member of AICROS