Analytical & Regulatory Chemistry, Inc.

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

A&A Pharmachem Inc. (founded 1992) is a leading Canadian supplier and distributor of:

- Pharmaceutical ingredients and regulatory compliance solutions
- Over the Counter ingredients products and ingredients
- Nutraceutical Ingredients
- Sports Nutrition Ingredients
- Food Ingredients

In the Pharmaceutical sector we represent many active pharmaceutical ingredient (API) manufacturers from India, China, and Taiwan as well as Western and Eastern Europe.

In the past 23 years, we have developed strong relationships with manufacturers of raw materials from Europe, India, China, US, South America, Japan. We can source and provide hard to find ingredients at cost effective prices. We differentiate from others by emphasizing on professional service and quality products, and by focusing on value creation for our customers.

Our portfolio of high quality Nutraceuticals Ingredients consists of Botanical Extracts and Powders, Specialty Ingredients, Amino Acids and Derivatives, Minerals, Vitamins, Sweeteners, Proteins, Enzymes and Blends, Vitamins and Blends, Excipients, Essential and Carrier Oils. We also stock substantial quantities of Whey Protein Concentrate, Whey Protein Isolate, Creatine Monohydrate, L-Glutamine and Branched Chain Amino Acids. In addition to the products listed on our site, we can source a wide range of specialized materials and formulations through our international network of suppliers. We act as a one stop shop by providing non-ingredient sourcing solutions such as packaging items, ranging from HDPE and PET packers and jars, to liquid and powder flavours.

Our distribution network covers entire North America through a network of 8 warehouses in Quebec, Ontario, Manitoba, British Columbia, New Jersey, Denver and Chicago. Our distributed operations enable us to deliver smallest to the largest orders efficiently and cost effectively.

I manage the Drug Product Manufacturing and Discovery Biology for Archer CPS. I serve multiple roles in Archer’s drug discovery, manufacturing and analytical work. My experience ranges from industrial to academic to non-profit environments, working in several fields including Chemistry, Biochemistry, Structural Biology and Drug Formulation. I have developed several immediate and modified release formulations of novel therapeutics and has completed Phase I manufacture of drug product in support of regulatory filings for Archer. I am actively engaged in collaborative efforts with Archer biologists to screen and validate novel drug compounds and targets in addition to overseeing drug formulation, manufacture, and analysis. I have developed many methods for small molecule isolation and characterization for drug discovery, as well as conventional quality control tests required for drug substance and drug product release and stability. I work closely with Archer CPS's Quality Services group in the preparation of the CMC sections for IND and IMPD submissions.

assainternational® was established in 1999 as a think tank and analytical resource to the pharmaceutical industry. Our mission is to offer international expertise in the many facets of solid-state characterization of pharmaceutical solids. As well as being a valued independent resource, we offer a variety of services that support the most current and up-to-date developments, innovations and technology.

assa® offers outstanding workshops and conferences on solid-state characterization of pharmaceutical material. The International Workshop on Solid-State Characterization of Pharmaceutical Solids (IWPCPS®) is known worldwide as the most comprehensive and up-to-date workshop of it’s kind.

assa® offers solid-state characterization of substances and formulations. We cover the whole range from early discovery phase to marketed products. We can also offer a unique inhalation know how.

Protecting intellectual property rights is one of the most critical tasks in pharmaceutical R&D. We work with international law firms to address your needs.

We can also assist you with setting up a complete, modern, solid-state characterization laboratory and provide assistance with the qualification or adherence (accreditation) of your laboratory to regulatory compliance codes.

assa® offers Business Services in marketing and sales issues to support the pharmaceutical industry, and all adjunct and related companies in related fields.

Avrio Biopharmaceuticals is dedicated to providing our clients with high quality, flexible and on time clinical trial material manufacturing services. Our experienced and dedicated staff and our world class facility allow us to provide our clients with timely solutions to meet the demand of early phase clinical trial material manufacturing.

Our newly commissioned, cGMP manufacturing facility offers a full range of services for your clinical trial material production.

Range of cGMP Support Services
Pre-formulation and Formulation Development
Small Molecules
Biopharmaceuticals

Parenteral Fill and Finish Manufacturing
Lyophilization
Blinding and Over-encapsulation
Packaging and Labeling
Regulatory Document Preparation
CMC Support
Clinical Supply Management
Complete Clinical Trial Support
Strategic Clinical Program Management
Clinical Protocol Development
Investigator Recruitment and Qualification
Clinical Study Management, Trial Monitoring and Data Analysis Preparation of Final Regulatory Submissions