What are the ways in which people can access the EBR?
From running a Trial. It depends on the scope of the trial.
Learn more: bit.ly/3Ad6hQ5
#ebr #electronicbatchrecord #pharma #trial #configuration
Looking for a reliable and affordable labeling and serialization solution for your global serialization needs?
Get to know more of our solutions: lnkd.in/eewBcJRH
#pharmaceutical #serialization #Aggregration #TrackandTrace
Factorytalk is an expert in providing GxP consulting services. Though our long experiences working with various companies, we have helped our customers to overcome their challenges.
Get to know more of our consulting services:
lnkd.in/gM4uqi2Z
#gxp #qms #csv #consulting
What’s new in GAMP Release 2? 🤔
Join our upcoming ISPE Malaysia webinar
on 23 Nov 20, 8.30 -11.15 AM, via Zoom to get all the answers.
🤗 Join now: lnkd.in/giQeYyZ3
#ISPEMalaysia #ISPEMYWebinar #GAMPR2 #CSV #goodpracticeupdate #MYISPE10 #ISPE
David Holt, Managing Director of Factorytalk, has joined in the Industrial Transformation Asia-Pacific (ITAP) event in Singapore.
For more detail > bit.ly/3N40O41
#event #nocode #industry40
Are you interested to join our fast-growing team at Factorytalk?
We have exciting job opportunities and currently look for new team members.
Opening positions are:
• Software Quality Specialist
• Business Analyst
• Senior Developer
Join our team now: lnkd.in/g4sd3uip
“BatchLine is great for Pharma companies like us looking to remove paper, control GMP risks, and improve overall performance in a simple and cost effective way”
Get to know more about our BatchLine EBR: factory-talk.com/it-solution…
#electronicbatchrecord #pharma #GMP #testimonial
Learn more about the EWI advantages and how it will fit into your manufacturing landscape: lnkd.in/g97-3vSP
#pharma #pharmamanufacturing #Tulip #lean # #kaizen
We will be at #ISPE Malaysia 10th Year Conference and Exhibition.
David Margetts, CEO of Factorytalk, will share his thoughts on new approaches to #GxP Digitization.
More details of the conference and register now to secure your spot to this session: bit.ly/3elLGSe
Research found that digital transformation and adoption of powerful digital tools are lagged behind in life sciences companies, with only 5% having widespread implementation. Here's why it is now time to plan on implementation an EQMS solution: bit.ly/3xl2Jug
#EQMS
One of Factorytalk successful eQMS projects with DBL Pharmaceuticals Limited in Bangladesh. Factorytalk is glad to be part of the eQMS software implementation that helps DBL Pharma products to comply with global regulatory standards.
Our next event is coming.
Join us at ISPE Malaysia 10TH Year Conference: Forging New Frontiers on 4-5 October 2022, at Royale Chulan, Damansara.
For more details >> bit.ly/3elLGSe
Key takeaways from our seminar
Update terkini terkait regulasi dan best practice yang perlu dipertimbangkan ketika perusahaan akan mengadopsi IT system modern (termasuk update GAMP 5 terbaru)
Find out more & Register now :
smpl.is/2t7s
#ISPEIndonesia #eQMS #EBR
Key takeaways from our seminar
Update terkini terkait regulasi dan best practice yang perlu dipertimbangkan ketika perusahaan akan mengadopsi IT system modern (termasuk update GAMP 5 terbaru)
Find out more & Register now :
smpl.is/2t7r
#ISPEIndonesia #eQMS #EBR
Get updated on the latest technology, digitization and IT approaches, and related regulatory insights in the GxP domain.
Space is limited to 50 participants, register now to secure your spot:
bit.ly/3JSvqUE
#ISPEIndonesia #pharmaceutical #seminar #GxP #pharma
CAPA is a way to make sure that a company is always doing its best and learning from its mistakes , and then change what you need to so that you can keep getting better and better.
factory-talk.com/knowledge/c…
Annex 11 of the European Union (EU) Good Manufacturing Practice (GMP) guidelines sets out the requirements for electronic signatures and batch release for medicinal products.
factory-talk.com/knowledge/a…
Compliance with 21 CFR part 11 is mandatory for all companies doing business in the United States.
21 CFR part 11 - FDA's requirements for electronic records and electronic signatures.
factory-talk.com/knowledge/2…