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Formulative (Industrial) Pharmacy – I Past Years RGUHS Download Question Paper PDF BPharmacy 5th Semester 2022

Formulative (Industrial) Pharmacy – I Past Years RGUHS Download Question Paper PDF BPharmacy 5th…

Regulatory affairs NOTES Download Notes PDF BPharmacy 7th Semester 2022

Regulatory affairs NOTES Download Notes PDF BPharmacy 7th Semester 2022📑 BP702T Industrial Phar…

Regulatory Affairs Industrial Pharmacy Handwritten IP-2 U-3 Download Notes PDF BPharmacy 7th Semester 2023

Regulatory Affairs Industrial Pharmacy Handwritten IP-2 U-3 Download Notes PDF BPharmacy 7th Sem…

Unit 5 Cosmetics Handwritten Notes Formulative Industrial Pharmacy Download Notes PDF BPharmacy 5th Semester 2022

Download PDF NotesBPharmacy 5th Semester PCI Download PDFUnit 5 Cosmetics Handwritten Notes Form…

Unit-1 Preformulation Studies Formulative (Industrial) Pharmacy Handwritten Notes Download Notes PDF BPharmacy 5th Semester 2022

Download PDF NotesBPharmacy 5th Semester PCI Download PDFUnit-1 Formulative (Industrial) Pharmac…

Unit-4 Parenteral Product Handwritten Notes Formulative Industrial Pharmacy Download Notes PDF BPharmacy 5th Semester 2022

Download PDF NotesBPharmacy 5th Semester PCI Download PDFUnit-4 Parenteral Product Handwritten N…

Biostatistics in Pharmaceutical Product Development | Industrial Pharmacy

Biostatistics in Pharmaceutical Product Development | Industrial PharmacyWhat is Biostatistics?S…

BP702T Industrial Pharmacy-II Notes B.Pharmacy 7th Semester Download PDF

BP702T Industrial Pharmacy-II NotesB Pharmacy 7th SemesterContent:
UNIT-I
Pilot plant scale up tec…

What is Spiking in Transfer of Technology (TOT) Industrial Pharmacy

Spiking:Spiking can be defined as the addition of unknown amount of a compound to a standard sam…

What is Quality Risk Management (QRM) in Transfer of Technology (TOT) Industrial Pharmacy

Quality Risk Management (QRM):Quality Risk Management is a systematic process for the assessment…

What is Process Validation in Transfer of Technology (TOT) Industrial Pharmacy

Process Validation:Process Validation is defined as the collection and evaluation of data, from …

What is Performance Qualification (PQ) in Transfer of Technology (TOT) Industrial Pharmacy

Performance Qualification (PQ):Document verification that the equipment or system operates consi…

What is Operational Qualification (OQ) in Transfer of Technology (TOT) Industrial Pharmacy

Operational Qualification (OQ):Document verification that the system or sub-system performs as i…

What is Installation Qualification (IQ) in Transfer of Technology (TOT) Industrial Pharmacy

Installation Qualification (IQ):The performance of tests to ensure that the installations used i…

What is GAP Analysis in Transfer of Technology (TOT) Industrial Pharmacy

GAP Analysis:Identification of critical element of a process which are available at the SU but a…

What is Sending Unit (SU) and Receiving Unit (RU) in Transfer of Technology (TOT) Industrial Pharmacy

Sending Unit (SU):The involved discipline at an organisation from where a designated product, pr…

What is Finished Pharmaceutical Product (FPP) in Transfer of Technology (TOT) Industrial Pharmacy

Finished Pharmaceutical Product (FPP):FPP or Finished Pharmaceutical Product can be defined as a…

What is Drug Master File (DMF) in Transfer of Technology (TOT) Industrial Pharmacy

Drug Master File (DMF):DMF or Drug Master File is teh detailed information regarding a specific …

What is Design Qualification (DQ) in Transfer of Technology (TOT) Industrial Pharmacy

Design Qualification (DQ):Design qualification is the document evidence that the premises, suppo…

CDSCO Industrial Pharmacy Notes PDF Download B.Pharm 7th Sem

CDSCO Industrial PharmacyNotes PDF DownloadB.Pharmacy 7th Semester