Ion Labs With over 27 years in tablet manufacturing, capsule manufacturing, and liquid manufacturing operations, Ion Lab's experience speaks volumes. The overriding value which sets us apart is our commitment to proactive...
Capsuline Capsuline’s sole purpose is to bring you the finest 2-piece hard shell gelatin, vegetable and flavored capsule products for you and your pets at the absolute lowest prices available anywhere.
Recognizing the need for a...
Capsugel Capsugel has emerged as a global leader creating innovative dosage forms for the pharmaceutical and dietary supplements industries. Companies look to our leadership to help them formulate new products, enhance existing...
Manesty OYSTAR Manesty is one of the world's leading pharmaceutical equipment companies, supplying the highest quality tablet manufacturing equipment to the international pharmaceutical industry for over 80 years. The OYSTAR...
Palmer Natural Products Palmer Natural Products is a full-service Contract Manufacturer and Private Label Supplier. We have decades of combined experience ready to help you from the concept stage to the market. We offer in-house formulation,...
Daiichi Sankyo, Inc. From the discovery of epinephrine to the development of the statin class of lipid-lowering agents, and the development of the first glitazone, which revolutionized long-term control of type 2 diabetes, the people of...
EVOXAC
EVOXAC is a capsule that is taken three times a day that may help salivary glands produce more saliva. With more saliva, the feeling of dry mouth may begin...
Azopharma Contract Pharmaceutical Services Azopharma specializes in drug development support for the pharmaceutical industry. We are experts at formulations, custom synthesis, isolation/purification, elucidation, characterization, method development and...
The core of any good clinical supply chain system is a supply management system that addresses all of the nuances of clinical supplies. Although Clinical Supply Management is often considered a back-office business unit for a sponsor, it is almost always on the critical path of the drug development process. The efficient, accurate and timely delivery of material to the investigators is critical ...
Common literature methods for determining formalde- hyde in air and water are based on derivatizing formalde- hyde first, by the use of either 2,4-dinitrophenylhydrazine (DNPH) or 2,3,4,5,6-pentafluorobenzyloxyamine (PFBOA) and then quantitating the resulting hydrazone or oxime. We report general procedures for the derivatization and determination of total extractable formaldehyde as well as ...
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 ...
Chemical categorization (or banding) of inherent toxicity and potency linked with defined safe work environments including exposure controls has become an integral component of assuring the health and safety of research workers and manufacturing personnel in the pharmaceutical industry but is not a substitute for quantitative risk assessment in the workplace.
While “going green” is a recent cliché, it is also a key factor to consider when developing a product or modifying a process. In today's economic climate, the regulated product manufacturer needs to perform a thorough cost-benefits analysis before considering such a change. The obvious benefit of going green is the environmental aspect. However, the potential competitive benefits need to be ...
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 ...
Capsules are incompatible with some fills. For instance, some for- mulations cause them to dissolve—almost seeming to melt—while others cause cracks to spontaneously form. While both effects stem A from an interaction between the fill and the capsule shell, crack formation requires the additional presence of mechanical stress on the shell. This article describes an investigation into how areas of ...
This article describes an investigation into why gelatin capsule
shells filled with hygroscopic materials sometimes crack. Its conclusions counter important aspects of the traditional theory.
As the popularity of liquid-filled hard capsules (LFHCs)
increases, formulators are becoming more interested in
ways to evaluate the compatibility of their formulations
with the capsule shell, ...
The Food, Drug and Cosmetic Act requires that a drug be the subject of an approved marketing application before it is transported or distributed across state lines. A sponsor however will want to ship an investigational drug to clinical investigators in many states; it must seek an exemption from that legal requirement. The Investigational New Drug Application (IND) obtains this exemption from ...
How to Guide for Writing a Drug Master File Introduction A drug master file (DMF) is a proprietary document typically written by or for the manufacturer to protect manufacturing information, an intermediate, starting raw material, Active Pharmaceutical Ingredient (API), description of production site/s or for other special requests. Most often, DMF's are written to protect the manufacturing ...
Watch this video to learn more about the Hyaluron Contract Manufacturing syringe filling system.
Inova H3-5V
1 mL long to 20 mL
up to 100,000 units per ...
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