Our Mission

To upgrade with diversified expertise in order to nullify risks topharmaceutical companies , clinical research organizations and end usersof medicines by ensuring quality, reliability, integrity and ethical values.

Our Vision

To bridge the gap between quality of medicines and indented results in patients.

Our Experience

  1.  Audited well known CRO’s Globally.
  2. Monitored 350+ Bio studies within multiple  therapeutic areas.
  3. More then 60 GCP Audits (Pre-qualification & Routine audits)
  4. More then 50 GMP Audits (Qualification of supplier & Routine audits)
  5. Serving to 20+ National & International customers (Generic and  Specialty pharma companies)
  6.  CDISC Projects 15+.
  7. IVIVR-IVIVC Analysis for 7+ molecules.
  8. USFDA Pre-inspection Audits with zero 483.
  9. Out Licensing Project with International sponsors.
  10. Review/Preparation of Module 4 & 5/Module 2.4 & 2.5

Our Services

Clinical Research

Clinical study design, review of Protocol, CRF, ICF, CSR, Statistical analysis/Randomization

GMP Audits

On site GMP Audits of Excipient/RM/PM/Medical devise GMP Audits manufacturer globally

Statistical services

Pk & Statistical Analysis, Randomization for Clinical studies , CDISC data set solution

Qualification & Routine

API/Formulation Manufacturer , Excipient/Raw material Manufacturer

Regulatory

Dossier Compilation including Module 2.4/2.5 writing Regulatory , Publishing

Additional

In/out licensing Additional , Consulting/Sourcing

Anacon Research is an emerging, Medium sized globally functional services provider with a depth of expertise in GCP, GMP, and GDP.

Anacon Research is an organization established with an aim of promoting safe medicines with highest standards to ensure intended results are achieved in patients and to shape the future of Pharmaceutical and Clinical research. This journey of ongoing experience has made Anacon Research fully aware and mature enough to offer and deliver best quality standards.

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ABOUT ANACON RESEARCH

  • Anacon Research is an emerging, medium-sized globally functional services provider with a depth of expertise in GCP, GMP, and GDP.
  • Anacon Research is an organization established with an aim of promoting safe medicines with highest standards to ensure intended results are achieved in patients and to shape the future of Pharmaceutical and Clinical research. This journey of ongoing experience has made Anacon Research fully aware and mature enough to offer and deliver best quality standards.
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Projects

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Our Value

Our Latest Articles

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Testimonials

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Jodi Thomas

Librarian
Jodi Thomas
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Lisa

Project Manager
Lisa

Pricing Package

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Team Work

Customer Service

Quality

Transparency

Integrity

Our Journey

2018
Started serving to Generic Pharmaceutical companies for Bioequivalence and Clinical trial-related activities.

▪ Clinical Monitoring
▪ Bioanalytical Monitoring
▪ Pre-inspection/CRO qualification Audit
▪ BA/BE Study Audits.
▪ RLD Sourcing

2019
Registered as a Pvt. Ltd. Company  &  Upgraded our service portfolio

▪ Statistical services including CDISC
▪ Support for Dossier In/Out-Licensing

▪ BE CRO Set-Up

2020
Service upgrade on sponsor request

▪ GMP Audits (API/Formulation/Raw/Packing Material).
▪ Support for patient based PK/PD studies and clinical trials.

2021
Upgrading service with diversified expertise

▪ IVIVC-IVIVR Analysis
▪ Patient based monitoring for Oncology trials
▪ Support for CMO , CDMO ,  F&D and R&D.

2023
Additional services.

▪ Patient based monitoring for Medical devise trials
▪ Additional statistical services for medical devise.