HomeEditorsChoice

  1. Drug Product Development Services
    6/30/2016

    Considering that 90% of drug candidates have bioavailability issues, making sure your program is prepared for all phases of clinical trials from the very start is the fast way forward. Patheon Solubility Enhancement Services approaches BCS II and IV drug substance solubility issues a fundamentally different way that identifies the solubility enhancement technologies most likely to work before you get started. That helps eliminate rework and worry later on.

  2. Pharmaceutical Development - Early Phase
    11/18/2016

    Almac’s experienced formulation scientists can develop a range of oral dose formulations for early stage clinical trials.

  3. G3Lab Universal SmartRocker Bioreactor System

    At Finesse, our goal is to enable customers to quickly and efficiently manufacture innovative drugs and vaccines. The SmartRocker, SmartBag, SmartPuck and SmartReader combination brings next generation control and measurement to rocking bioreactor applications. A SmartRocker is controlled by a G3Lab™ Universal SmartController and Finesse TruBio® software. This turnkey package provides a complete solution for research, process development, or seed train production applications.

  4. Drug Product CGMP Lyophilization Manufacturing Services
    11/1/2016

    Emergent BioSolutions currently fills a number of lyophilized products in its two 240 ft2 lyophilizers.

  5. Market Research Report: Small Molecule API Contract Manufacturer Quality Benchmarking (2nd Edition)
    7/14/2017

    This market research report is based off of the data provided from 241 respondents who have been involved in outsourced small molecule projects over the past 18 months. It provides service quality evaluations on 36 CMOs across 27 critical attributes. These attributes include: Proven ability to manufacture small molecule API, Reliable on-time delivery, Strong regulatory track record, Track record for meeting quality performance metrics, Ability to smoothly scale up manufacturing and transfer technology, Scientific knowledge, among others. The respondents provided assessment ratings based off of 689 total service encounters.

  6. Biologics Contract Development
    7/1/2016

    Comprehensive contract development. Reliable cGMP manufacturing. Gain a competitive advantage in both by choosing Patheon for your biopharmaceuticals and biosimilars. You’ll have access to end-to-end, fully integrated services for both drug substances and drug products, delivered on time and on budget. A simplified supply chain that accelerates development and keeps you ahead in the rapidly changing world of biologics.

  7. Drug Process Development
    4/26/2016

    Althea’s complete range of drug Process Development capabilities offers the tools to address your needs. We develop processes for producing small quantities of proteins for early testing or establish robust, reliable and scalable processes that enable a strong commercial advantage. Althea also provides access to a proprietary drug delivery platform, called Crystalomics® technology, for the development of alternative drug delivery formulations of second generation drug substances.

  8. Cell and Gene Therapy Logistics
    3/31/2017

    Cell and Gene Therapies have demonstrated real promise as they move into the clinical trial phase for a variety of life changing and deadly diseases. The results of these studies and their potential impact to patients, their loved ones and the industry as a whole are almost incalculable, which makes securing the supply chain mission critical — though not easily accomplished. What makes World Courier so essential for Cell and Gene Therapy logistics is our understanding and our ability to address these critical issues.