CXR Biosciences: the investigative and exploratory toxicology company (now Concept Life Sciences)

Founded in 2004, Pharmaron is a cutting-edge, fully integrated pharmaceutical R&D service platform supporting the life science industry. The company has invested in its people and facilities and established its comprehensive service offerings throughout the pharmaceutical R&D lifecycle. With operations in China, the US and the UK staffed by more than 11,000 employees, Pharmaron has an excellent track record in delivering end-to-end R&D solutions to its partners globally and enabling them to accelerate their novel drug discovery and development process.

Pharmaron is a contract research organization (CRO).

Services:
* Synthetic, medicinal and analytical chemistry services
* Biology services
* DMPK services
* Pharmacology services
* Drug safety assessment services
* Radiochemistry and isotopically labelled metabolism services
* Chemical & pharmaceutical development services
* Clinical development services

www.pharmaron.com

CRO - Contract Research Organization
Library Synthesis
CADD
Bioorganic Chemistry
Discovery Process Chemistry
Radiolabelled Chemical Synthesis
ChemInformatics
in vitro Biology
in vitro Screening
Structural Biology
in vivo Pharmacology
Animal Disease Models
ex vivo Pharmacology
Biomarkers
in vitro ADME
in vivo PK
PKPD
QA
Regulatory Affairs
Discovery Biologics
Process Chemistry
API Manufacturing
Material Science
Formulation Development
Drug Product Manufacturing
Toxicology
Safety Pharmacology
Genetic Toxicology
DART
Pathology
Immunotoxicity
Bioanalytical
14C / Carbon-14 Radiosynthesis
3H / Tritium Radiosynthesis
QWBA
mARG
Clinical AME
Mass Balance
Metabolite Profiling
Microdosing Phase 0
Absolute Bioavailability
DDI
First-in-Human (FIH)
Thorough QT(TQT)
Ethnobridging

BIONEEDS INDIA PRIVATE LIMITED is a Bangalore based Contract Research Organization providing Integrated Discovery, Development and Regulatory Services to Pharmaceutical,
Biopharmaceutical, Agrochemical, Industrial chemical, Herbal/Nutraceutical and Medical device companies.

Accreditation/Certifications
• National GLP Compliance Monitoring Authority (NGCMA), Dept. of Science and Technology, Government of India
• Committee for the Purpose of Control and Supervision of Experiments on Animals (CPCSEA), Ministry of Environment, Forests and Climate Change, GOI.
• State Drug Controller as a Government approved Drug Testing Laboratory for carrying out tests on Drugs / Cosmetics and
• Raw Materials used in their manufacture on behalf of licensees for manufacture for sale of drugs / cosmetics
• Review Committee on Genetic Manipulation (RCGM), department of biotechnology, GOI to conduct experiments on animals for DNA or Genetically modied resources
• Bioneeds is AAALAC certified for laboratory animal care
• Bioneeds’ in-house R & D unit is recognised by Department of Scientic and Industrial Research (DSIR)
• ISO 17025 certified for Biological evaluation of Medical Devices
• Bioneeds has best-in-class infrastructure equipped with state-of-the-art facilities with 2,50,000 sqft built-up area.
• Vivarium with 85 exclusive animal rooms built as per international standards
• Cutting edge Drug Discovery and Development Labs to support Medicinal chemistry, Biology, In vivo Pharmacology,
• Toxicology, Custom synthesis, Process R&D, cGMP manufacturing, Formulation and Analytical development services

CSBio is a leading peptide and peptide synthesizer manufacturing company located on the edge of Silicon Valley in Menlo Park, California. Since 1993, CSBio has been providing high quality custom peptides, cGMP peptides and automated peptide synthesizers to the global biotech community. Our peptide products and peptide synthesis equipment can be found in peptide production laboratories and pharmaceutical companies worldwide.

CSBio now also offers solid phase peptide synthesis resins as well as high quality Fmoc and Boc protected amino acids for use in both R&D and cGMP peptide manufacturing. Our state of the art cGMP manufacturing facility provides cGMP peptides for preclinical and clinical programs and our commercialization and regulatory teams can take you from toxicology studies through market commercialization. Our product line also includes a complete list of generic peptide APIs including the most widely used peptide APIs in the industry. Whatever your peptide requirements, CSBio can assist you in reaching your ultimate goals by offering high quality products and world class support.

We are ChemPartner, an innovative, full-service life science CRO/CDMO providing biopharmaceutical research with a global reach. We have evolved from a chemistry service provider to a company offering full-service drug discovery and development for both small and large molecules, supported by biology, pharmacology, DMPK, and exploratory toxicology.

We are dedicated to technically and strategically accomplishing the research initiatives of pharmaceutical and biotech companies worldwide. Our mission is to provide clients with the highest quality R&D services in a timely and cost-effective manner.

As a Contract Research Organization (CRO) ChemPartner has helped hundreds of clients take their small molecule and biologics projects from all stages of drug discovery to pre-clinical candidate selection and beyond. We provide assistance not only in laboratory settings but also intellectual input at various levels, such as project strategy, experimental study design, data interpretation, and source reports for regulatory filings.

As a Contract Development and Manufacturing Organization (CDMO), we offer pharmaceutical development and manufacturing services for small molecules and biologics. We provide one-stop services for overall process development and IND application support, with a quality system in compliance with ICH guidelines and the highest standards of the CFDA, FDA, and EMA. We have expanded our Biologics GMP manufacturing capacity in our new facility in Qidong, suitable for commercial drug substance or products.

ChemPartner is uniquely positioned to not only be a CRO/CDMO, but to be the most reliable pharmaceutical alliance partner providing intellectual contributions and exceptional technical expertise.

The SafeBridge Regulatory & Life Sciences Group is the premier resource for high-level safety and health consulting to the pharmaceutical and biotechnology industry. Founded in 1997, the team includes more than 50 professionals who provide the Potent Compound Safety Triangle® of services, namely, toxicology, industrial hygiene, and industrial hygiene analytical chemistry. Our specific expertise is in the recognition, evaluation, and control of potential worker exposure and product safety issues associated with the handling of potent and highly potent drug substances and drug products. In addition to the work we have traditionally performed for the pharmaceutical industry, we also provide services related to the registration and approval of food and beverage ingredients and biocides, general industry industrial hygiene services, quality assurance of non-clinical toxicology studies, and regulatory submissions for the registration of industrial and specialty chemicals for global trade (e.g., REACH, TSCA).

---How We Can Help You---
We can provide occupational health hazard and qualitative and quantitative exposure assessments to support the R&D and manufacture of potent compounds in the pharmaceutical industry by applying our expertise in toxicological health-based risk assessments, process hazard assessment, and industrial hygiene analytical chemistry. We can help you obtain regulatory approval of food and beverage ingredients and biocides with expertise from staff that joined through the acquisition of Toxicology Regulatory Services (TRS). And, we can help you with global trade support with expertise from staff that joined through the acquisition of the Redstone Group. Together, our technical team provides experienced and knowledgeable scientific and regulatory expertise that is proven, reliable, and highly respected.