Certificate Course in Pharmaceutical Microbiology

Description

Pharmaceutical microbiology is an applied branch of microbiology. It involves the study of microorganisms associated with the manufacture of pharmaceuticals e.g. minimizing the number of microorganisms in a process environment, excluding microorganisms and microbial byproducts like exotoxin and endotoxin from water and other starting materials, and ensuring the finished pharmaceutical product is sterile. Other aspects of pharmaceutical microbiology include the research and development of anti-infective agents, the use of microorganisms to detect mutagenic and carcinogenic activity in prospective drugs, and the use of microorganisms in the manufacture of pharmaceutical products like insulin and human growth hormone.

Course Details:

Instructor Name: Bhavana Tatineni

Instructor Qualification: Master of Science (Microbiology)

Instructor experience: 18+ years experience in quality control microbiology  at various pharmaceutical industries.

Course Syllabus:

1.      Introduction to Pharmaceutical microbiology

2. Flow of Microbiology laboratory and Facility design

3. Media receipt, storage, preparation

4. Media growth promotion test and qualification

5. Culture handling

6. Types of water systems in pharma industry, validation overview

7. Water sampling, testing, and trending of data.

8. Types of Environmental monitoring, and data trending

9. Environmental monitoring location selection criteria and risk assessments.

10. Microbial Limit Test

11. Bacterial Endotoxin Test

12. Sterility testing

13. Bioassays of Antibiotics and Vitamins

14. Preservative efficacy testing

15. Analytical method validations in Microbiology

16. Types of Equipment's/instruments and its uses in Microbiology laboratory

17. Sterilization techniques and validation of autoclave.

18. Handling of biological indicators and its qualification.

19. Microbiological monitoring of gases (Nitrogen and compressed air)

20. Disinfectant validation

21. Sterile manufacturing facility and Media fills

22. Handling of OOS in Microbiology.

23. Cleaning validation and handling of clean room Bioburden samples.

24. Handling and destruction of Biological waste.

25. Identification of microorganisms.

26. Biopharmaceuticals

27. Microbiology best laboratory practices

28. Guidelines for Microbial testing.

29. Data integrity and data mapping.

How this course can benefit your career:

The "Certificate Course in Pharmaceutical Microbiology" equips individuals with essential knowledge and skills relevant to various career paths within the pharmaceutical industry.

Here's a brief description of how this course can benefit your career:

1. Quality Control and Assurance Roles:

   • Gain a deep understanding of microbial contamination control, sterility testing, and environmental monitoring, essential for roles in quality control and assurance departments.

2. Research and Development:

   • Learn about microbial identification techniques, antimicrobial susceptibility testing, and bioburden determination, valuable for research and development of new pharmaceutical products.

3. Regulatory Affairs:

   • Acquire insights into regulatory requirements and guidelines related to microbial testing and validation, crucial for ensuring compliance with regulatory standards.

4. Manufacturing and Production:

   • Understand the principles of aseptic processing, cleanroom classification, and microbial limit testing, essential for roles in pharmaceutical manufacturing and production.

5. Pharmaceutical Sales and Marketing:

   • Enhance your understanding of microbiological concepts and terminology to effectively communicate with healthcare professionals and customers in sales and marketing roles.

6. Consultancy and Training:

   • Develop expertise in pharmaceutical microbiology to offer consultancy services or conduct training sessions for pharmaceutical companies, academic institutions, or regulatory agencies.

7. Career Advancement Opportunities:

   • Obtain a recognized certification that validates your expertise in pharmaceutical microbiology, enhancing your credentials and opening up new career advancement opportunities.

Overall, the "Certificate Course in Pharmaceutical Microbiology" provides a solid foundation in microbiological principles and practices tailored to the pharmaceutical industry. Whether you are a student aspiring to enter the industry or a professional looking to advance your career, this course equips you with the knowledge and skills needed to succeed in various roles within the pharmaceutical sector.

Microbiological Quality Control of Pharmaceutical Products:

Contamination of pharmaceutical products by objectionable microorganisms is a major risk within the pharmaceutical industry as it may impact product integrity and patient safety. To prevent contamination events from occurring, licensed pharmaceutical manufacturing companies worldwide are required to adhere to strict regulations and robust quality control procedures issued by their respective government agencies. These regulatory processes and procedures comprise various quality control methods, such as those described in the United States Pharmacopeia (USP), European Pharmacopeia (EP), and Japanese Pharmacopeia (JP). When properly followed, these procedures can help identify microbial contamination prior to product release, thus avoiding the pitfalls of product recalls.

Microbiological quality control is an essential part of the pharmaceutical manufacturing process. Pharmaceutical companies must safeguard the quality and safety of their products by thoroughly testing raw materials, equipment, environmental surfaces, and final preparations for microbial contaminants that may have been introduced inadvertently during or subsequent to the manufacturing process. Currently, there are a number of microbiological quality control assays recommended, including growth promotion testing, microbial enumeration testing, and antimicrobial effectiveness testing. Growth promotion testing, for example, is a common quality control assay used to establish the nutritional properties of culture media to ensure that microbial growth can be supported. This form of testing is important because culture media is frequently employed in various pharmacopeial quality control assays. If a batch of media is found to be unable to support microbial growth, the results of all assays for which the media was intended will be unreliable, and the pharmacopeial tests will fail.

Following growth promotion testing of culture media, approved batches of media can be used in other quality control assays such as the microbial enumeration test (USP <61>) or the antimicrobial effectiveness test (USP <51>).1,2 These particular tests are designed to determine whether a pharmaceutical product complies with an established specification for microbiological quality or demonstrates effective antimicrobial protection, respectively. In particular, the microbial enumeration test is recommended to ensure that the product contains less than the allowable concentration of an objectionable organism via direct plating, membrane filtration, or the most-probable-number method. In contrast, the antimicrobial effectiveness test is performed to confirm that the antimicrobial preservatives added to the final product are demonstrating an effective level of microbial growth inhibition.

What You Will Learn!

• Flow of Microbiology laboratory and Facility design
• Media receipt, storage, preparation
• Media growth promotion test and qualification
• Culture handling
• Types of water systems in pharma industry, validation overview
• Water sampling, testing, and trending of data.
• Types of Environmental monitoring, and data trending
• Environmental monitoring location selection criteria and risk assessments
• Microbial Limit Test(MLT)
• Bacterial Endotoxin Test
• Sterility testing
• Bioassays of Antibiotics and Vitamins
• Preservative efficacy testing
• Analytical method validations in Microbiology
• Types of Equipment's/instruments and its uses in Microbiology laboratory
• Sterilization techniques and validation of autoclave.
• Handling of biological indicators and its qualification
• Microbiological monitoring of gases (Nitrogen and compressed air)
• Disinfectant validation
• Sterile manufacturing facility and Media fills
• Handling of OOS in Microbiology.
• Cleaning validation and handling of clean room Bioburden samples
• Handling and destruction of Biological waste
• Identification of microorganisms
• Biopharmaceuticals
• Microbiology best laboratory practices
• Guidelines for Microbial testing.
• Data integrity and data mapping.

Who Should Attend!

• Graduate or postgraduate degree in Pharmacy or Pharmaceutical Sciences
• Graduate or postgraduate degree in Chemistry (subject) .
• Graduate or postgraduate degree in Microbiology
• Graduate or postgraduate degree in Biotechnology

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