Why Zetalix ?

Who Are We

Zetalix is an independent CRO offering World class services to the Pharmaceutical, Nutraceuticals, and Biotechnology industries in various stages of drug development.
Zetalix management & operations team brings considerable experience in conducting Clinical Trials on the patient populations on various dosage forms including injectables like IM/IV/SC, oral dosage forms, liquid formulations, topical preparations, Trans-dermal Patches/ metered dose inhalers, etc.
The Clinical studies conducted at Zetalix are fully GCP compliant & strong SOP-driven culture ensures compliance with all statutory and mandatory requirements.
Zetalix emphasizes safety and ethical work practices while assuring you with the highest standards in terms of data integrity and regulatory compliance.
Zetalix has the capability to recruit subjects for study specific needs like Hypertensive patients, Gynecology, Cancer patients, etc. through partnerships with Investigators, Hospitals, and Clinics.

We offer a wide range of services.

Regulatory Affairs.
Clinical Operations.
eCRF Development.
Data Management. Consultancy in GMP/GLP.

Our Strength

  • Manage Global as well as domestic clinical trials with precision and perfection.
  • Having Comprehensive project management team, quality expert management team and potential site coordinators
  • Timely execution of sponsors/CRO requirements
  • Potential Investigators and sites
  • Faster Patient Recruitment
  • Maintaining quality of the data
  • Resolving and responding to all the queries within timelines
  • Strict compliance with study timelines and protocol
  • Work with a variety of sponsor’s compounds
  • Effective communication
  • Compliance with FDA, local regulatory and ICH-GCP guidelines

Why Zetalix ?

  • We present qualified, pre-screened, Principal Investigators for participation in clinical trials in virtually any specialty area.
  • We ensure timely and accurate regulatory board submission and data collection.
  • We provide access to a large patient study population.
  • We provide ongoing and effective communication between Sites, Investigators and Customers.

Our mission is encapsulated in providing a conducive system for clinical trials, experiments & observational studies, tailored to specific requirements, to respond to rising burden of diseases & growing demand for innovation in drugs and medical devices.

We envision ourselves going beyond the development of new drugs, diagnostic tools & treatments, to contributing in planning of healthcare services, facilitating continuous evaluation & progress of medical care, with a thorough investigation of risk-factors.

Our Team

  • Highly experienced and receptive team 5 to 10 years experience in the Pharmaceutical industry
  • Well trained and potential staff (ICH-GCP, ICMR, ScheduleY and FDA regulations)
  • Experience with all phases of clinical trials (Phase II -IV) across multiple therapeutic areas, in both paper and EDC environments
  • Immaculate track record for delivery on time and with quality