A leading global provider of enterprise quality management software and services for the Life Sciences and other highly regulated industries.
Tampa, FL
Joined May 2009
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#Pilgrim Quality Solutions is now #IQVIA Quality Compliance. Find our same dynamic content at linkedin.com/showcase/iqvia-… - IQVIA’s Integrated Global Compliance Showcase.
Stay in touch and discover how IQVIA’s #compliance offerings support our customers from concept to market.
Customer success in the #LifeSciences depends on establishing a collaborative partnership between #technology solutions providers and their customers. Follow these key steps to maximize the success of your technology engagement. #IQVIA pilgrimquality.com/blog/guid…
Purpose-built #GMP #AssetManagement software provides the necessary functionality to both manage #compliance risks and drive productivity for #lifesciences organizations. hubs.ly/H0m3rYl0
LIVE WEBINAR DECEMBER 5, 11AM (EST) - Learn how integrated #AssetManagement and #Quality Management Systems (#QMS) help improve #GMP compliance efforts, reduce quality risks, and increase overall productivity. REGISTER NOW: hubs.ly/H0m2hpP0
#MedicalDevice regulatory requirements underscore the importance of maintaining an ongoing #Quality Management process, as regulations dictate that device makers provide documented evidence of executing a well-defined #designcontrol process. hubs.ly/H0lF7390
Visit #IQVIA at the #American Medical Device Summit 2019 #MedTechUS19 in Chicago, October 28-29. Stop by Booth 12 to learn about our range of integrated global #compliance solutions. #MedTechUS19
With less than 8 months to go to the full application of #EUMDR in May 2020, there are still only 5 #NotifiedBodies designated to the MDR. If your NB isn’t designated yet, have a back-up plan in case that NB fails or is designated too late. hubs.ly/H0lprP90
As you prep for the looming #EUMDR compliance requirements, this round-up of blogs offers insight into components of the #medicaldevice product lifecycle that you need to consider to asses if you’re ready for the May 2020 deadline. hubs.ly/H0l7zvR0
Visit #IQVIA at #TheMedTechConference in Boston through 9/25. Stop by Booth 333 to learn about our range of integrated global compliance solutions. Enter our raffle for an opportunity to win a 2-day customized #MDR & #Quality #Compliance Readiness Assessment Review.
When a #LifeSciences organization decides to implement new processes or solutions, the greatest predictor of its success will be how it manages the psychology of #change. hubs.ly/H0kX1ph0
Visit #IQVIA at #TheMedTechConference in Boston through 9/25. Stop by Booth 333 to learn about our range of integrated global #compliance solutions.
Visit #IQVIA at #RAPS Regulatory Convergence 2019. Stop by Booth #326 to learn about our range of #RegulatoryIntelligence and #QualityCompliance solutions and services.
Visit #IQVIA at #RAPS Regulatory Convergence 2019. Stop by Booth 326 to learn about our range of #RegulatoryIntelligence and #QualityCompliance solutions and services.
#LifeScience organizations are now recognizing there is opportunity for innovation in #quality, #regulatory, safety, and commercial compliance activities that will drive up both the perceived and the actual value of #Compliance from concept to market. hubs.ly/H0kHvPV0
The right #QMS vendor will facilitate the production of superior goods and services, while also continuously supporting #regulatorycompliance. That’s why the QMS vendor vetting process is a critical first step toward success. pilgrimquality.com/blog/pros…
At the highest level of maturity, organizations begin developing a true #cultureofquality with end-to-end #quality processes and the ability for #metrics to help sustain and improve overall quality. hubs.ly/H0kmf5G0