Home
About Us
Pharmaceutical Industry
Research & Development
Regulatory Affairs
Quality Assurance
Quality Control
Production Department
Project Management
Environmental, Health & Safety (EHS)
Computer System Validation
Microbiology
Pharma SOPs
QA SOP’s
QC SOP’S
Microbiology SOP’s
Production SOP’s
General SOP’s
Clinical Research
Pharmacovigilance
Medical Coding
Courses
Videos
Job Notifications
Select Page
Engineering Department
Home
Engineering Department
Engineering Department
“Role of Air Handling Units (AHUs) in Pharmaceutical Cleanrooms: Ensuring Product Safety and Compliance”
Dr. Yashashwini Reddy
October 24, 2024
No Comments
Engineering Department
Role of Engineering Department in Pharmaceutical Industry
Dr. Yashashwini Reddy
October 9, 2024
No Comments
Engineering Department
“HVAC Systems in Pharmaceuticals: Ensuring Optimal Conditions for Quality and Compliance”
Dr. Yashashwini Reddy
September 24, 2024
No Comments
Engineering Department
,
Quality Assurance
“Understanding the Importance and Types of Clean Rooms in Pharmaceutical Manufacturing”
Dr. Yashashwini Reddy
September 23, 2024
No Comments
Engineering Department
Understanding Pharmaceutical Waters
Dr. Yashashwini Reddy
July 11, 2024
No Comments
Engineering Department
,
Production Department
What is Factory Acceptance Test ?
Dr. Yashashwini Reddy
July 1, 2024
No Comments
Engineering Department
,
Production Department
SAT – Site Acceptance Test
Dr. Yashashwini Reddy
May 16, 2024
No Comments
Engineering Department
Popular Categories
Clinical data Management
(4)
Clinical Research
(5)
Clinical SAS
(1)
Computer System Validation
(8)
Engineering Department
(7)
Environmental, Health & Safety (EHS)
(7)
General SOP’s
(1)
Medical Coding
(11)
Microbiology
(13)
Microbiology SOP’s
(3)
Pharmacovigilance
(28)
Pharma SOPs
(98)
Production Department
(210)
Production SOP’s
(6)
Project Management
(1)
QA SOP’s
(1)
QC SOP’S
(4)
Quality Assurance
(92)
Quality Control
(214)
Regulatory Affairs
(43)
Research & Development
(41)
Warehouse
(4)
Recent Post
Guideline on good pharmacovigilance practices (GVP): Module XVI Addendum II – Methods for evaluating effectiveness of risk minimisation measures
Guideline on good pharmacovigilance practices (GVP) Module XVI – Risk minimisation measures
Guideline on good pharmacovigilance practices: Module XV – Safety communication
Guideline on good pharmacovigilance practices: Module X – Additional monitoring
Guideline on good pharmacovigilance practices (GVP): Module IX – Signal management
Hello
Chat now via Whatsapp
