DYNALABS LLC

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.

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

BioChroma Analytical Labs LLC is based out of the DFW metroplex in the heart of Texas. It was created to fill the technical gaps in new product development for innovators with new ideas that might not have all the necessary components to make it happen and to offer support for product quality through analytical testing and consulting. We provide an all-encompassing service to help our clients develop a product that is continually manufactured to the level of quality customers expect. Our goal is to provide continual scientific and technical support for entrepreneurs and established businesses based on quality at an affordable price. We are here to provide technical assistance to foster their idea from inception to the marketplace and beyond.
We have experience and expertise in research and development, formulations, scale-up, testing, quality and regulatory of a wide variety of consumer products in the areas of cosmetics, skin care, topical and oral OTCs, food, beverages, dietary supplements, household cleaners and the like.

Product Research and Development: Skin, Body, Hair Care Development, Dietary Supplement Development

Consulting: Packaging Advice, Manufacturing Advice, Plant Inspections, Ingredient Stability Advice, Container Closure Advice, Product Formulation Advice, Quality and Regulatory Advice

Chemistry Analysis: Nutritional Analysis, Mineral Analysis, Vitamin Analysis, Preservative Analysis, Active Ingredient Analysis, Allergen Analysis

Microbiological Analysis: General Microbiology Analysis, Pathogenic Bacteria Analysis, Spoilage Organism Analysis, Preservative Efficacy Analysis, Bacterial Challenge Studies, In vitro Time-Kill Studies, Antibiotic Studies, Water Suitability Testing

Laboratory Research and Development: Transdermal Studies, Antimicrobial Efficacy, Product Specific Studies Aimed at Demonstrating Efficacy or Quality

DSA Consultants: Your Partner for Regulatory Affairs & GMP Quality Compliance.

If your company provides manufacturing, packaging, wholesale, distribution or importing services, your company is responsible to ensure compliance with the Canadian Food & Drugs Act.

DSA Consultants address every aspect of Drug, Medical Device, Natural Health Product and Cosmetic compliance.

At DSA Consultants, we know that in order to be successful, you can’t be everything to every arm of the healthcare industry. We only provide consulting services and aren’t distracted by other business activities.

Contact DSA Consultants for more information about how we can assist you.

IRISYS, LLC. founded in 1996, has grown from a small laboratory focused on formulation development to an organization that provides a full spectrum of pharmaceutical product development contract services designed to move compounds from early research to Phase I/II clinical trials. Recro® acquired IriSys in August 2021.
Recro® is a bi-coastal contract development and manufacturing organization (CDMO) with capabilities spanning pre-Investigational New Drug (IND) development to commercial manufacturing and packaging for a wide range of small molecule therapeutic dosage forms. With expertise in solving complex manufacturing problems, Recro is a leading CDMO providing primarily small molecule therapeutic development, end-to-end regulatory support, clinical and commercial manufacturing, aseptic fill/finish, lyophilization, high potency compound development, packaging, and logistics services to the global pharmaceutical market. In addition to our experience handling DEA controlled substances and developing and manufacturing modified release dosage forms, Recro has the expertise to deliver on our clients’ pharmaceutical development and manufacturing projects, regardless of complexity level. We do all of this in our best-in-class facilities, totaling 145,000 square feet, in Gainesville, Georgia, and San Diego, California.