Pharmaceutical Production & Manufacturing
What do you learn in the Pharmaceutical Production & Manufacturing Course? Pharmaceutical Manufacturing Processes Good Manufacturing Practices (GMP) Quality Control and Assurance Packaging and Labeling Regulatory Compliance Process Optimization Safety Protocols Emerging Technologies Industry-specific Software Environmental Sustainability Who Should Learn …
What do you learn in the Pharmaceutical Production & Manufacturing Course?
- Pharmaceutical Manufacturing Processes
- Good Manufacturing Practices (GMP)
- Quality Control and Assurance
- Packaging and Labeling
- Regulatory Compliance
- Process Optimization
- Safety Protocols
- Emerging Technologies
- Industry-specific Software
- Environmental Sustainability
Who Should Learn Pharmaceutical Production & Manufacturing Course?
- Pharmaceutical Professionals
- Aspiring Manufacturing Technicians
- Quality Control and Assurance Personnel
- Regulatory Affairs Specialists
- Pharmacy Graduates
- Chemical Engineers
About this Certificate Course
The Diploma in Pharmaceutical Production & Manufacturing is a comprehensive program aimed at providing in-depth knowledge and practical skills in pharmaceutical manufacturing. This course covers a wide range of topics, including pharmaceutical manufacturing processes, Good Manufacturing Practices (GMP), quality control, regulatory compliance, packaging, and labelling. Students gain hands-on experience in a simulated manufacturing environment, enabling them to apply their knowledge effectively. The curriculum also emphasizes emerging technologies and sustainability in pharmaceutical manufacturing. Graduates of this diploma program are well-prepared for roles in pharmaceutical production, quality assurance, and regulatory compliance, making them valuable assets in the pharmaceutical industry.
Certify Yourself & Stand Out!
- Showcase your skills
- Gain a competitive edge
- Stand out to recruiters
- Land your dream job
Why should you take the Pharmaceutical Production & Manufacturing Course?
Taking the Pharmaceutical Production & Manufacturing course is essential for those aiming to excel in the pharmaceutical industry. This program equips you with the expertise required for pharmaceutical manufacturing, ensuring you understand the intricacies of production processes, quality control, and regulatory compliance. With the pharmaceutical sector’s growing demand for skilled professionals, this course opens doors to rewarding career opportunities. Whether you’re an industry professional seeking advancement or a newcomer aspiring to enter pharmaceutical manufacturing, this course empowers you with the knowledge and skills to thrive in this vital field.
Curriculum
- 5 Sections
- 29 Lessons
- 16 Weeks
- UNIT-I9
- 1.1Overview of Pharmaceutical Industry.Copy
- 1.2Introduction to different departments and their roles and Good Industrial Practices.Copy
- 1.3Facilities and Equipment system overviewCopy
- 1.4Manufacturing process, unit operation, Packing and labelling of Dosage Forms (Tablets, Capsules, Liquid Orals, Injectable Semisolids/Ointments)Copy
- 1.5Quality Assurance- Role and responsibilitiesCopy
- 1.6In-process checking /samplingsCopy
- 1.7Quality ControlCopy
- 1.8IPQC test: Dissolution test, DT, Friability, Drug contents determination, Moisture contents of granules, Weight variation of uncoated tablets, Hardness testCopy
- 1.9Different types of document s and their usesCopy
- UNIT-II5
- 2.1Overview of basic skills and importance of a Chemist- Production (Pharma, Cosmetics & Biologics) in a Non-Sterile product manufacturing processCopy
- 2.2Introduction of functional and cross-functional stakeholders for Chemist – Production (Pharma, Cosmetics & Biologics)Copy
- 2.3Various communication methods (verbal and written) for reporting incidents/ deviations.  Strategies for manpower management and optimization of team productivityCopy
- 2.4Introduction of various type of audits in the life sciences sector for the manufacturing operations.Copy
- 2.5Introduction of the Sexual Harassment of Women at Workplace (Prevention, Prohibition, and Redressed) Act and the provided penalties for violation at workplaceCopy
- UNIT-III5
- 3.1Importance of Standard operating procedures, equipment master list, and equipment qualification plan for production process.Copy
- 3.2Process of calibration and validation of the equipment and balances used in the manufacturing area.Copy
- 3.3Different types of pre-production checks performed in a production unit.Copy
- 3.4Various troubleshooting methods and solutions for guidance to operators during production activities in consideration of critical process parameters and critical quality attributes.Copy
- 3.5Role of assay and Quantity effect in biopharmaceutical formulation.Copy
- UNIT-IV5
- 4.1Various method of reporting and documentation as per Good Documentation Practices (GDP) and other regulatory guidelines.Copy
- 4.2Introduction of Attributable, Legible, Contemporaneous, Original, and Accurate Plus (ALCOA PLUS) principle and its importance.Copy
- 4.3Overview and introduction of Drug Master File (DMF), Batch Manufacturing Record (BMR) and Batch Packaging Record (BPR).Copy
- 4.4Industrial practices for generation of electronic and manual records in the log-books and other documentation required as per GMP and GDP.Copy
- 4.5Management of Batch Manufacturing Record (BMR) and Batch Packaging Record (BPR) for each intermediate and finished non-sterile product.Copy
- UNIT-V5
- 5.1Introduction to working principle of machines and equipment used for various non-sterile product manufacturing process like tablet, capsule, liquid oral and their calibration and validation process.Copy
- 5.2Introduction of ICH Q7 GMP guidelines for non-sterile product manufacturing.Copy
- 5.3Application of various pharmaceutical and engineering concepts for troubleshooting in manufacturing process related to machines and equipment for tablet, capsule, and liquid orals.Copy
- 5.4Process of cleaning validation for a non-sterile production area and equipment.Copy
- 5.5Concept and procedure of root cause analysis for out-of-specification (OOS) and out-of-trend (OOT) products in case of deviations in production process.Copy
