• Open Hours: Mon - Sat 9.00 - 18.00
  • +49 1575 7819 326
  • info@clinizig.com

Welcome To Clinizig

Clinical SAS Excellence, Globally Trusted

At Clinizig GmbH, our success is built on a highly qualified team with a strong scientific foundation and deep expertise in clinical research. We operate in strict alignment with international quality standards and guidelines, while remaining flexible to meet client‑specific requirements. Whether through full‑service execution in collaboration with our trusted CRO partners or by working seamlessly with client‑appointed teams, we ensure reliable project delivery and success. Registered with the Local Court of Leipzig, Germany (Commercial Register HRB 40144), Clinizig GmbH has been economically active since 12 April 2022. With over 4 years of operational experience, we support pharmaceutical and CRO companies through our Functional Service Provider (FSP) model — offering Statistical Programming, SDTM, ADaM, TLFs, and Biometrics support. Today, our team of approximately 80 Biostatistics and Statistical Programming professionals contributes to global clinical development projects across multiple therapeutic areas, positioning Clinizig as a trusted partner for enterprises worldwide.

Research Capabilities.In pharmaceutical research, we offer
  • Pre-clinical studies.
  • Clinical studies (Phases I–IV).
  • Post-marketing studies
  • Observational studies

Our Clients

Questions

Frequently Asked Questions?

Find answers to common inquiries regarding our statistical programming methodologies, data security protocols, and clinical trial reporting standards.

We follow a rigorous implementation process that includes automated validation using Pinnacle 21, manual double-programming, and a thorough review of Define.xml files. This ensures your data is fully compliant with FDA and PMDA submission requirements from day one.

Our "Gold Standard" process involves independent double-programming for all primary and secondary endpoints. We perform a detailed reconciliation of outputs and ensure a 100% match between the lead and validator programmers before any deliverable is finalized.

Yes. Our team has extensive experience in preparing Clinical Study Reports (CSRs), Integrated Summaries of Safety (ISS), and Integrated Summaries of Effectiveness (ISE). We provide the full eCTD-compliant package, including programs, datasets, and technical documents required for successful filing.

Our Testimonials

What Our Patients Say

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Cameron Steve

Houston Director

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John Doe

Heart Patient

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Cameron Steve

Houston Director

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John Doe

Heart Patient

Looking For Consultation?

+49 1575 7819 326

Reliability is built on experience. The CLINIZIG team possesses a rich history of over 20 years in a wide range of therapeutic areas, positioning us as a highly reliable partner for both small-to-medium enterprises and global pharmaceutical players.