Patheon Inc. Patheon Inc. is a leading global provider of contract development and manufacturing services to the pharmaceutical industry. Patheon prides itself in providing the highest quality products and services to more than 300...
Solids
With over thirty years of experience in manufacturing a wide range of solid dosage forms, Patheon is equipped with the experience and expertise necessary to...
Cephalon, Inc. A global biopharmaceutical company driven to expand the boundaries of science to improve human health. A company with first-in-class therapeutics, a rich oncology research pipeline and medications to treat central nervous...
AMRIX
AMRIX® (Cyclobenzaprine Hydrochloride Extended-Release Capsules) is indicated as an adjunct to rest and physical therapy for relief of muscle spasm...
FENTORA
FENTORA® (fentanyl buccal tablet) [C-II] is indicated only for the management of breakthrough pain in patients with cancer who are already receiving and...
NUVIGIL
NUVIGIL® (armodafinil) Tablets [C-IV] is indicated to improve wakefulness in patients with excessive sleepiness associated with treated obstructive sleep...
Agere Pharmaceuticals Inc. Agere Pharmaceuticals, Inc. was established to provide state-of-art solutions to the development of poorly soluble compounds. Agere integrates comprehensive scientific knowledge and formulation expertise with innovative...
SoluForm™
Insoluble API places special demands on solid dosage forms. For example, for immediate release applications it is critical that dosage forms dissolve...
TetraGenx TetraGenx was formed in 2000 providing pharmaceutical development and consulting services to the North and Central American markets.
As the corporation grew, additional complimentary services and staff members were...
Dosage Forms
TetraGenx has developed a wealth of knowledge and experience as a result of its expert staff. Periodically, new and experienced staff members are taken on...
AccuChart The products available from AccuChart include 4 types of solid unit dope/bar code packaging systems- the Cadet, the Cadet Twin, The Cadet Twin 2x2, and the Punch Cadet- all for tablet and capsule unit does/bar code...
AAIPHARMA Services. Our services include: clinical packaging/distribution, solid dose & sterile contract manufacturing, analytical services, formulation development for solids and liquids, validation services, regulatory affairs and oral...
cGMP manufacturing services
AAIPharma Services provides cGMP manufacturing services for clinical and commercial products at its solid dosage and sterile product manufacturing...
ProCR™
ProCR™ is a matrix tablet formulated with a combination of three commercially available polymers.
Prolipid
Proprietary Self Emulsification (SEDDS, SMEDDS) System
Hercules Inc./ Aqualon Div. Aqualon has been delivering pharmaceutical performance since the 1950s. To find out more about Aqualon's products for pharmaceuticals, typical applications, our technical support resources, and contact for sales and other...
Crystal engineering provides a rational approach to solving formulation, processing and product performance problems. This review discusses how the concept of crystal engineering can be judiciously utilized to manipulate the solid-state properties of
drugs and excipients for successful pharmaceutical formulation and process development.
Existing and emerging manufacturing as well as ...
An Alternative Approach to Bioequivalence Studies for Semi- Solid Dosage Form Products
Bioequivalence Study Requirements for Semisolid Dosage Form Products
The guidance on Scale-Up and Post Approval Changes (SUPAC)1 for drug products is an informal document representing the best current scientific judgments of the FDA. Its intended purpose is to lower the regulatory burden on the industry ...
The formulation of drugs into capsules is often utilized in early phase development due to the relatively quicker formulation-development process. The bioavailability of the poorly soluble drugs can be significantly increased when formulated in a solubilized form in a capsule (i.e. liquid or semi-solid filled capsules). Acidic degradation and dyspeptic side effects associated with some compounds ...
The zeta potential (ZP) is a function of the surface charge which develops when any material is placed in a liquid. It is a very good index of the magnitude of the electrostatic repulsive interaction between particies. The ZP is commonly used to predict and control dispersion stabiliry. The characteristics of the solid-liquid interface may also influence, inter alia, adhesion, flotation and, in ...
THE SCORR: Although this campaign has received national advertising awards for its cre- ative merit and execution, the true measure of success is in a return on invest- ment for Camargo. In that regard, it has exceeded all expectations.
The “old dog, new tricks” approach served to solidify Camargo’s standing in the industry as experts in 505(b)(2) and continues to be the platform from which the ...
In an era characterized by the need to continuously evaluate and bolster R&D pipelines, the increasing complexity and overall cost to develop and approve drug products, the trend toward genericization, and mounting pressures to both decrease prices and maximize profitability, the pharmaceutical industry has sought competitive advantage in lower cost manufacturing jurisdictions.
The ...
Powder & Porous Materials Characterization
Powder Density in Solid Dosage Forms B by: Martin A. Thomas Ph.D., Director of Business Development Quantachrome Instruments (martin.thomas@quantachrome.com) Both active and inactive (excipient) compounds nal or tapped state. In free-owing powders the are used in the manufacture of solid dosage initial bulk and tapped densities will be more ...
Dissolution is an important test method that is carried out on solid oral dosage forms like capsules, tablets, and oral suspensions. For these dosage forms to be efficacious, the active drug substance must be absorbed into the systemic circulation so that it can be transported to its site of activity. The overall efficiency of this process contributes to the bioavailability of the drug substance ...
the stability of a lyophilized igG1 monoclonal antibody was investigated using suboptimal levels of the lyoprotectant, sucrose and the incorporation of the plasticizer, sorbitol. after lyophilization, aggregation and sub-visible particle formation in the reconstituted formulations were evaluated by a number of techniques chosen to encompass a wide range of aggregate sizes. these methods included ...
Formulation is arguably the most critical—and challenging—component of biopharmaceutical drug development, second only to the molecule itself. Formulation's far-reaching consequences help sponsors satisfy the scientific, medical, and regulatory conditions for drug approval and, subsequently, support marketplace success.
A biopharmaceutical formulation consists of active pharmaceutical ...
The miVac Duo is suitable for use with a wide range of solvents, from volatile organic solvents through to water and some of the higher boiling point ...
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