Products
Case study
11-Apr-2013 -
Pharmaceutical manufacturers worldwide are turning to vision inspection as a way to safeguard their brands, keeping products with label and packaging defects from retailer shelves. One major pharmaceutical manufacturer came to Mettler-Toledo CI-Vision hoping to reduce the rate of defective...
Technical / white paper
26-Mar-2013 -
The goal of method validation is to provide proof that data from each individual sample is indicative of the actual batch content with little deviation. This paper outlines the importance of validation as well as the official requirements, including characteristics...
On-Demand Supplier Webinar
25-Mar-2013 -
2013 Industry trends driving the scientific, logistical and regulatory complexity of supply chain industry
Implement clinical development methodologies for quality, relationships, and performance
Strategies to optimize drug development to reduce global trial time and costs
On-Demand Supplier Webinar
06-Mar-2013 -
What are the regulators telling us?
Dealing with a non-harmonized, multi-agency, global challenge.
Monsters Vs, Aliens
How to navigate the maze of import & export regulators.
Thinking beyond the box!
Packaging selection – A different horse for every course
Validation & Qualification – Where are...
On-Demand Supplier Webinar
06-Mar-2013 -
How to determine if a depot or direct to site shipments are more efficient
Calculation based on a case study
How to avoid delays and assure that your shipments arrives without delays and excursions
Technical / white paper
26-Feb-2013 -
This whitepaper describes three scenarios that clearly demonstrate the value TruScan brings to pharmaceutical manufacturing facilities and the underlying benefits of implementing TruScan that make such extensive savings possible.Each case study provides an in-depth examination of the deployments of TruScan...
Technical / white paper
04-Feb-2013 -
An extractables and leachables case study describes how a comprehensive risk assessment was performed across the entire production process of a European manufacturing plant for 40 finished products, resulting in a global testing plan
Insight guide
26-Sep-2012 -
Collaborative partnering between Contract Development and Manufacturing Organizations (CDMO) and the drug product submission applicants is becoming increasingly important with the emphasis on product design by regulatory agencies.The CDMO can provide the appropriate resources to build the scientific knowledge base...
Data sheet
17-Sep-2012 -
Radio Ion ChromatographyPositron emission tomography (PET) is one of the most powerful noninvasive diagnostic tools for tracing organ functioning. Quality control of the short-lived PET-radiopharmaceuticals is challenging, not least because of the tough time limits, the radiation issue and the near nanomole radiotracer...
On-Demand Supplier Webinar
22-May-2012 -
This webinar will give you a better understanding of how the end of one-size-fits all medicine, and current oncology drug developments in diagnosis and biomarkers positively impact clinical trials. It will also address key oncology drug development barriers and best...
On-Demand Supplier Webinar
22-May-2012 -
Clinical trials in the Asia Pacific are increasing exponentially. Numerous sponsors and CROs have accessed this region in recent years to take advantage of high performing, cost effective sites. To many sponsors though, Asia Pacific appears an impenetrable black box....
On-Demand Supplier Webinar
22-May-2012 -
Clinical trial in Oncology involves one of the most expensive and complex protocols in a research environment. For the past few years, Latin America has been included in the scenario of this study area due to its patient’s recruitment potential,...