Product news > Contract services (outsourcing)
Technical / white paper
Glycosylation of Proteins: Structure & Analysis - SGS
06-Dec-2011 -
Glycosylation is one of the most widely observed, and structurally diverse, forms of post-translational modification of proteins and glycans have been shown to have a range of specific biological roles.
Mass spectrometry-based techniques provide an extremely powerful tool for glycan...
Technical / white paper
Ensuring Quality & Regulatory Compliance when Working with a CDMO - DPT
24-Oct-2011 -
Learn the three elements needed to ensure regulatory compliance & product safety, purity and potency.
Careful choice of your service provider
Effective partnership management
Mutual commitment to constant improvement
Data sheet
Partnering with Your CDMO for CMC Preparation - DPT
04-Oct-2011 -
Collaborative partnering between Contract Development and Manufacturing Organizations (CDMO) and the drug product submission applicants (Applicant) is becoming increasingly important with the emphasis on product design by regulatory agencies. The CDMO can provide the appropriate resources to build the scientific...
On-Demand Supplier Webinar
Continuous Process Improvement for Solid Oral Dose Development - Colorcon
22-Aug-2011 -
Need to improve team collaboration and save time bringing products to market? Then don’t miss this insightful webinar to learn how to expedite excipient selection, transform product design, and achieve product differentiation to gain competitive advantage.
Technical / white paper
Vetter – Pharma solutions for tomorrow, today. - Vetter Pharma International GmbH
08-Jun-2011 -
With fewer blockbuster drugs in the pipeline, companies are on the lookout for an enduring solution to meet market challenges. These include rising process costs resulting from stricter quality control criteria, evolving technologies, which are becoming more complex and costly,...
Event programme
How Will You Innovate? - Biologics-Drug Delivery Sys Dev & Lifecycle Mgmt
17-May-2011 -
Have you been asked to innovate and don’t really know where to start? Learn key concepts and get hands-on experience developing innovative approaches to improve supply chain performance and increase market share at the DCAT/ISM Sourcing Summit on July 13...
On-Demand Supplier Webinar
Are you getting the right bioavailability and bioequivalence data for inhalation products you’re developing? - DPT
16-May-2011 -
Consider the risk to your development program of not accounting for patient variation in device handling. In this webinar DPT Labs and Proveris Scientific team up to demonstrate how the Ergo system can help you develop the right actuation parameters...
Data sheet
Key steps to consider when working with a cdmo to identify optimal packaging options - DPT
08-Mar-2011 -
There are many factors to take into consideration when selecting or designing a packaging component. Steps involved during the initial stage of the process are extremely important in ensuring that the most optimal packaging is identified. Working with a contract...
On-Demand Supplier Webinar
Diversity for catalysts – assuring speedy and versatile solutions for scale up success - DSM Pharmaceutical Products
03-Feb-2011 -
Wondering how DSM’s unique collection of thousands of catalysts leads to speedy and versatile solutions for scale up success? We will show you how broad chemical and biological diversity increases the chance to successfully identify catalysts
Technical / white paper
White Paper on Residual DNA-Based Services - SGS
31-Jan-2011 -
Accurate quantification of residual DNA at each purification step of a biopharmaceutical is essential. This paper outlines the analytical procedures available to measure this residual DNA and the advantages and drawbacks to each.
Technical / white paper
Custom Manufacturing Driven by Core Competencies at Genzyme Pharmaceuticals - Genzyme Pharmaceuticals
05-Oct-2010 -
With global competition in custom manufacturing dramatically shifting, companies are changing business strategies to extend geographic presence, create low-cost production capacities, develop investment-intensive chemistry capabilities, or further leverage existing economies-of-scale.
Genzyme Pharmaceuticals’ custom manufacturing business is based on long-standing competencies...
Case study
Five year trouble free manufacturing for large pharma company - Alkermes
23-Sep-2010 -
Alkermes, through the merger with Elan Drug Technologies,to become Alkermes plc,has been developing and manufacturing commercial scale solid oral dosage products for over 40 years.This case study demonstrates a large pharmaceutical contract manufacturing engagement in which there has been five...
Technical / white paper
The 10 Essential Don’ts for Manufacturers to combat Main Street’s ‘New Normal’ and win - CDC Software
10-Sep-2010 -
Many factories are currently engaged in many cost reduction initiatives that are stumbling or have dramatically slowed down. In many cases they continue because received wisdom supposes that they must deliver a benefit otherwise we would not be doing them....
Technical / white paper
Beyond Plant Visibility to Business Improvement - CDC Software
17-Aug-2010 -
Increasing evidence is pointing to the realization that many plant-wide intelligence initiatives do not lead to the dramatic improvements that the business wants and needs.
This Cambashi Analyst White Paper discusses five major factors that producers must incorporate into their...
Technical / white paper
Generate Sales Leads: Free White Paper - William Reed Business Media
02-Aug-2010 -
White papers (or technical papers) are one of the most effective ways to generate leads for your sales team and establish your company’s reputation as a thought leader. Want to know how to create an effective white paper? Download William...
Survey
Are you Asking the Right Questions? - William Reed Business Media
02-Aug-2010 -
Want to evaluate your company’s brand image or the opinion of the Outsourcing-Pharma readers on a certain topic? Want to perform a market research analysis without the hassle? Download William Reed Business Media’s survey brochure to find out how you...
Case study
Characterization of hydrolysates to enhance CHO cell culture process understanding - SAFC Pharma
06-Jul-2010 -
Undefined components, such as protein hydrolysates, are routinely used in biopharmaceutical production to boost the growth and productivity of cells in culture. Due to regulatory concerns and variability associated with these components, a need for chemically defined basal formulations has...
Technical / white paper
Five keys to reducing time-to-market - Vetter Pharma International GmbH
27-Apr-2010 -
With development times measured in years, increasing costs represent a major challenge confronting pharmaceutical and biotechnology companies. As a result, reducing time-to-market is an essential component in any business strategy, particularly when the end of patent protection is considered. One...
Case study
Fermentation Technology: Cooking Up New Therapeutics - SAFC Pharma
14-Apr-2010 -
Fermentation technology offers the pharmaceutical industry a reliable, powerful and economic source for chemical and biological therapeutic drugs.
Silvian Shama, Business Development Manager at SAFC’s new $29 million cGMP fermentation facility in Jerusalem, Israel, demonstrates the growing diversity of applications...
Technical / white paper
PHARMACEUTICAL GAS ANALYSIS: A NEW TREND IN THE REGULATORY FOCUS - SGS
31-Mar-2010 -
More attention is being focused on gases role as an excipient in pharmaceutical development. Download SGS’s Technical Bulletin and learn more about cGMP monitoring and quality testing including contamination control...
Technical / white paper
Generate sales leads with a good white paper - William Reed Business Media
24-Mar-2010 -
White papers (or technical papers) are one of the most effective ways to generate leads for your sales team and improve your company’s reputation as an expert. Want to know how to create effective white papers? Download this guide now.
...
Technical / white paper
An Introduction to High-Potent API Classification - SAFC Pharma
12-Nov-2009 -
When dealing with highly potent compounds, it’s critical that failsafe procedures are in place relating to their handling, storage and containment. In order to ensure that the correct procedures are installed and adhered to, a logical system of classifying the...
On-Demand Supplier Webinar
Meet the requirements for GSDP for pharmaceutical products - SGS
12-Oct-2009 -
SGS
invites you to attend a free webinar to gain an overview on how to ensure the quality and integrity of your pharmaceutical products during all aspects of the storage and distribution process.
Technical / white paper
Handling Protocols Key Consideration in HPAPI Market - SAFC Pharma
18-Sep-2009 -
Over the past 10 years, the manufacture of highly potent active pharmaceutical ingredients (HPAPIs) has become increasingly attractive to contract manufacturers due to significant advances in clinical pharmacology and oncology research. In addition, with factors such as fewer FDA drug...
On-Demand Supplier Webinar
Shoot for share: from vial to pre-filled syringe - Baxter
08-Jul-2009 -
Pre-filled syringes are a growing alternative to vials for many of today’s parenteral products. According to recent estimates, the market for pre-filled systems is expected to top 2.4 billion by 2010. The increased interest in pre-filled syringes is in large...
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On your radar
Globalisation
- China healthcare spending up despite economic fears, BD says
- FDA calls for more powers to adopt nationwide ePedigree
Lifecycle management
- Samsung and Quintiles' biosimilars JV teams with Biogen Idec
- Ongoing quality problems at injectables plant hurt Hospira in Q3
Counterfeiting
- Annual WHO meeting to tackle spread of substandard drugs
- FDA calls for more powers to adopt nationwide ePedigree
