Life Sciences eBook: Reducing Cycle Time with Digital Transaction Management
Paper and manual processes are delaying critical treatments from getting to market. Discover how Life science organizations reduce development...
Going Mobile with Electronic Signatures
With more and more professionals using mobile phones and applications, the \"mobile wave\" is impacting every business function across...
Embracing a Collaboration Network Model for Discovery Research
Life sciences companies are fundamentally changing the way they operate by routinely externalizing non-core competencies to external partners and...
Following FDA Guidance -Continuous Improvement in an Outsourced Environment
Many organizations face growing needs to outsource operations to contract manufacturing organizations (CMOs). Meanwhile, the FDA continues to enact...
The State of Environmental Monitoring – Avoiding the Dire Risks of a Poorly Executed Program
To better understand the challenges managers face every day when it comes to Environmental Monitoring programs, BIOVIA (previously Accelrys)...
How to Avoid the Top 5 LIMS Nightmares
Because current traditional LIMS have not delivered on their promise, many organizations are still searching for solutions to optimize...
7 Things You Must Know When Selecting an Electronic Lab Notebook
Electronic lab notebooks (ELNs) allow researchers to easily store, search and share experiment data from any location—but selecting the...
Streamline Regulatory Compliance in Life Sciences with Digital Transaction Management
Leading life sciences companies aim to improve health outcomes around the world by delivering breakthrough treatments while complying with...
Latin America: Regulatory Compliance Requirements for Life Science Products (Focus: Brazil, Mexico, Argentina): 2-day In-person Seminar
This two-day comprehensive Course on Latin America Regulatory compliance requirements will cover topics ranging from pre-clinical and clinical requirements...
Lifescience Seminar Catalogue
This is a catalogue on all GRC seminars conducted on the topic LifeScience in San Fransisco during First quarter...
How to Avoid the Top 5 Lims Nightmares
Traditional Laboratory Information Management System (LIMS) implementations are notorious for keeping people awake at night. Because traditional LIMS have...
Following FDA Guidance: Continuous Improvement in an Outsourced Environment
Many organizations face growing needs to outsource operations to contract manufacturing organizations (CMOs). Meanwhile, the FDA continues to enact...
Embracing a Collaboration Network Model for Discovery Research
Technology Spotlight: IDC Health Insights Today, Pharma companies spend almost one third of their global research budgets with external...
The State of Environmental Monitoring: Avoiding the Dire Risks of a Poorly Executed Program
Effective microbiological and environmental monitoring (EM) is a mission-critical priority for pharmaceutical and biotechnology drug manufacturing and packaging operations....
How to Avoid the Top 5 Lims Nightmares
Traditional Laboratory Information Management System (LIMS) implementations are notorious for keeping people awake at night. Because traditional LIMS have...
Building a Vendor Qualification Program for FDA Regulated Industries
If you are looking for the answer to the following questions, you will certainly benefit from attending this seminar...
Ensuring Compliance with Advertising and Promotional Requirements for Drugs and Medical Devices
Federal regulation of the advertising and promotion of pharmaceuticals and medical devices reflects an aggressive attitude on the part...
Statistical Considerations for ICH Guidelines: 2-day In-person Seminar
This 2 day hands-on workshop explores the unique challenges facing all facets of a pharmaceutical and biotechnology company. Practical...
How a Scientific Data Management System Will Help Cut Costs & Boost Productivity
A pharmaceutical manufacturer was struggling with turnaround times and human errors due to the fact that their laboratory was...
