Electronic submissions for IND Safety Reports to FAERS
Blog Electronic submissions for IND Safety Reports to FAERS Key Highlights Starting June 28, 2021,...
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After 15 years in the industry, we decided to alter direction. Now, we share our passion by helping others. Our ramp-up process is designed to empower your team.
We believe in Partnering together, to create value for our esteemed Clients in an ethical and transparent manner to advance the science of zealous pharmacovigilance, thereby meeting the regulatory requirements.
M-Lite Solution eliminates the manual process to prepare R2/R3 ICSR formats.
SOP’s, so that all Clinical data from different database sources can be reconciled
Case line report from clinical trial DB. Generate segregate report template.
Convert R3 files received from one Regulatory Authority/Partner to R2 format.
Talk to our team today.
- Specialized Support Team to help Business and IT Operations - Annual Subscription Model of the Services
- Safety Database Hosting on the Cloud - Back-up Database Hosting on the Cloud
- SME Team to help Business and Project Specific needs - Project-based Subscription model of the Services
- Regulatory Affairs Consulting
Blog Electronic submissions for IND Safety Reports to FAERS Key Highlights Starting June 28, 2021,...
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Olcay have been proven partner for all our pharma needs.
Olcay is our technology partner for regulatory reports.
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Olcay Tech team is not only well experienced but also expertise in design, development and delivery in just in time. This makes Pharma company life easy.
Olcay is one stop solution provider for all Pharmacovigilance needs of any Pharma company like preparation, automation, operations, reports.
Yes, we have been delivering best tailormade solutions to ensure right technology for your needs. Most of our customers see good ROI working with us.
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