Abiogenesis Clinpharm Private Limited is an emerging contract research organization (CRO) that provides client specific services in clinical development of drugs and devices. Our research wing helps clients in clinical development program of drugs and devices at every step. Our expertise comes from an experienced team of professionals having credentials of successfully conducting national and international clinical trials across all phases of clinical development. Abiogenesis Clinpharm Private Limited is capable of delivering quality work from early proof of concept to late phase development including post launch product lifecycle management.
We are a team of highly skilled people having expertise in the area of clinical research and work experience in leading clinical development programs of many reputed organizations. Our team epitomise scientific knowledge and operational excellence in clinical research industry. We have the ability to integrate the primary concept of clinical development into project management plan with micro level execution strategies. We have direct operating experience from initial planning to project execution from Phase I to Phase IV studies in different therapeutic areas across the globe. Our expertise should be utilised in following services.
Accelsiors is a scientifically-driven, global, full-service Contract Research Organization (CRO). We support the Pharma industry globally to accelerate and manage every activity across clinical drug development.
Since 2002, we have been committed to providing Sponsors working in highly complex disease indications with the scientific knowledge, regulatory expertise and quality operations necessary to achieve their development objectives.
Accelsiors expertise includes studies in the following areas:
Accutest, a global independent and internationally accredited Contract Research Organisation (“CRO”), with more than 20 years of experience and over 700+ employees in supporting the end-to-end services for global bio-pharmaceutical, biotech, medical device, nutraceutical and FMCG companies. Accutest is the market leader among independent CROs, with the highest quality standards and quick turnaround times. We have a strong regulatory track record and numerous accreditation/approvals from global regulatory agencies.
We offer services in 3 verticals:
1. Bio-availability and Bio-equivalence studies (BA/BE) -
2. Clinical Development Services (CDS)- Phase II - IV studies, Post marketing, Investigator initiated & stand alone services (medical writing, regulatory consultancy, clinical data management)
3. Biologics Services - Solutions for biosimilars, novel biologics and non-biological complex generics
Successfully cleared below inspections:
USFDA – 33 times (latest Nov, 2018)
WHO – 23 times (latest Jan, 2019)
DCGI- 20 times (latest Oct, 2016)
EMA – 8 times (latest Dec, 2017)
Actimus Bio is an Clinical Research Organisation (CRO)
Actimus Bio is pioneering a novel approach by addressing the needs of the pharmaceutical and biotech industry and partnering the development of medicines for the future.
Actimus Bio facility is approved by Drugs Controller General of India (DCGI).
Actimus Bio is a full service BA/BE CRO dedicated to meet the needs of pharmaceutical and biotechnology companies.
Actimus Bio offers an extensive range of Clinical services including
o Study design,
o project management,
o Medical safety monitoring,
o Quality assurance auditing,
o Regulatory submissions and scientific communications
AGINKO Research is the premiere CRO for preclinical work in osteoarticular pathologies. We offer a wide range of contract research services to support Drug and Medical Device established companies as well as start-ups and academia. From industry standard protocols to customized research design, our animal models and assays, both on an in vivo or in vitro basis, provide key tools for compound discovery and product development.
Given our expertise, know-how, and network in the field of osteoarticular pathologies, AGINKO today also offers a full range of histology services for your preclinical and clinical trials as well as general consulting services (e.g., regulatory, strategy, financing) devoted to osteoarticular pathologies.