ADM Pharmaceuticals

ADM logo

Quality & Compliance – From Source to Final Product

With more than a century of experience, dedicated production lines and specialized R&D and regulatory teams, ADM offers its customers innovative global solutions tailored to the specific challenges of the pharmaceutical industry. At ADM, we offer a range of products that meet major relevant pharmaceutical regulations and are manufactured according to appropriate cGMP standards. We make delivering compliance and consistency a reality, giving you an edge to innovate with confidence. We are committed to providing only the purest and highest quality products for your end solutions.


Our Product Ranges

ADM has an extensive range of products to meet your pharmaceutical needs, all manufactured under strict quality and regulatory conditions to ensure compliance. Our products can be used in a wide range of pharmaceutical applications.

PharmaEdge Ingredients
(API’s and Parenteral Excipients)

pharmaedge ingredients teaser image

The PharmaEdge products are manufactured under cGMP standards and are supported with Certificates of Suitability to the European Pharmacopoeia (CEPs) and/or FDA Drug Master Files (DMFs).

PharmaPlus Ingredients
(Oral & Topical Excipients)

The PharmaPlus products are compliant with the specifications of the EP and USP monographs.

Fully & Partially Hydrogenated Soybean Oils (VGB 4S & shortening 36)

Refined Pharma Oils (Soybean, Sesame, Sunflower, Rapeseed and Olive)

pharmaplus ingredients - capsules and tablets

Carbohydrates
Dextrose/ Glucose Monohydrate
Fructose
Maize / Corn Starch
Wheat Starch
Sorbitol Liquid (70%)
Maltitol Liquid

Lecithin’s
Soy lecithin, fluid or de-oiled (powder)
Canola/Rapeseed Lecithin
Sunflower Lecithin
Capsulec Series – (high choline content)

Glycerol & Propylene Glycol
Bioethanol (high purity)
Citric Acid Anhydrous Powder USP FCC


Regulatory Conformity and Quality Standards

ADM has regulatory expertise in the fields of pharmaceutics, food and cosmetics. Our regulatory team provides continuous regulatory services in order to comply with your product requirements. Our production and quality control system fulfill the cGMP requirements appropriate for the production of active pharmaceutical ingredients and excipients. We work closely with manufacturing site to manage variability and guarantee batch-to-batch consistency.

With ADM providing the best solutions and practices for the sourcing of starting materials used to produce pharmaceutical ingredients, we aim at delivering the very best solutions to fit the requirements of the pharmaceutical industry.


Brochures

Refined Olive Oil IV Sell Sheet_1
Sell Sheet – Refined Olive Oil IV
Sell Sheet – Refined Sesame Oil IV-1
Sell Sheet – Refined Sesame Oil IV-1
Sell Sheet – Refined Soybean Oil IV
Sell Sheet – Refined Soybean Oil IV
Sell Sheet – Fully Hydrogenated Soybean Oil VGB 4S
Sell Sheet – Fully Hydrogenated Soybean Oil VGB 4S
Specification Sheet – Dextrose
Specification Sheet – Dextrose
Specification Sheet – Fructose
Specification Sheet – Fructose
Specification Sheet – Native Corn / Maize Starch
Specification Sheet – Native Corn / Maize Starch
Specification Sheet – Native Wheat Starch
Specification Sheet – Native Wheat Starch
Whitepaper – Refined Sesame Oil IV-1
Whitepaper – Refined Sesame Oil IV-1
Whitepaper – Managing the natural variability of plant-based pharmaceutical ingredients
Whitepaper – Managing the natural variability of plant-based pharmaceutical ingredients
Whitepaper – Use of high melting point solid vegetable oils in encapsulation processes
Whitepaper – Use of high melting point solid vegetable oils in encapsulation processes
Whitepaper – Pharmaceutical oils for cannabinoid drug products

Contact

ADM
16 rue du Général de Gaulle
62223 Saint-Laurent-Blangy
France


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