I’m looking forward to showing all the medical device, biotech and pharmaceutical companies all the advantages of utilizing Salesforce for GxP processes and why they don’t need to worry about security or compliance with government regulations.
SANTA BARBARA, CALIFORNIA (PRWEB) April 28, 2015
USDM Life Sciences, a leading global regulatory consulting firm in the life sciences industry, is proud to partner with Salesforce.com to present a webinar, Validate Salesforce and Move Your GxP Processes to the Cloud.
Numerous medium to large life sciences organizations are realizing the huge potential and power of moving their GxP processes to Salesforce. But, some life sciences organizations worry that data in a cloud environment, such as Salesforce is not secure or compliant with government regulations. In reality, data in the Cloud can be safe and compliant with regulations, including 21 CFR Part 11.
“I’m looking forward to showing all the medical device, biotech and pharmaceutical companies all the advantages of utilizing Salesforce for GxP processes and why they don’t need to worry about security or compliance with government regulations,” said David Blewitt, Vice President of Cloud Compliance Services and Solutions at USDM Life Sciences.
The webinar will include an overview of Salesforce security, how data can be compliant, how Salesforce can be validated and highlight some of the many processes life sciences organizations are accomplishing with the powerful cloud based CRM system. Attendees will hear from industry leading experts on security and cloud compliance who specialize in solutions for life sciences organizations. Attendees also will have an opportunity to get all of their security and compliance questions answered.
The complimentary webinar is on Thursday, April 30 at 11am PDT/2pm EDT. Visit the webinar registration page to save your spot for this exclusive event.
About USDM Life Sciences:
USDM Life Sciences is a leading global regulatory consulting firm providing compliance, validation, qualification, quality, auditing and information technology services via project teams and staff augmentation to our clients in the medical device, biotechnology, biologics, diagnostics and pharmaceutical industries. USDM Life Sciences has more than 15 years of experience supplying our clients in the life science industry with compliance services during each phase of their drug and product development cycle while partnering with best of breed organizations to help companies simplify, unify and optimize their business and compliance objectives. For more information, please visit http://www.usdm.com.