Introduction, Regulatory requirements for validation, Role of FDA, Code of Federal regulation, Validation life cycle, Significance of validation, Types of validation, Process valiadation, Phases of process validation, Process capability design, Process Qualification, Validation maintainance phase
Types of Process validation, Examples
Objectives of CGMP
Layout of buildings, services, equipments & maintenance
Production organization
material management
handling and transportation
inventory management &control
Production and planning control
Sales forcasting
Budget and cost control
Industrial and personnel relationship
Total quality management
Introduction, Regulatory requirements for validation, Role of FDA, Code of Federal regulation, Validation life cycle, Significance of validation, Types of validation, Process valiadation, Phases of process validation, Process capability design, Process Qualification, Validation maintainance phase
Types of Process validation, Examples
Objectives of CGMP
Layout of buildings, services, equipments & maintenance
Production organization
material management
handling and transportation
inventory management &control
Production and planning control
Sales forcasting
Budget and cost control
Industrial and personnel relationship
Total quality management
QUALIFICATION & VALIDATION.Validation is an essential part of GMP, and an element of QA.Critical steps in the process need to be validated.Need for confidence that the product will consistently meet predetermined specifications and attributes.
Quality control on secondary packaging materialsAnupriyaNR
Presentation on quality control tests for the secondary packaging materials. Includes the materials used for secondary packaging, ideal properties of the secondary packaging material and various test procedures used for the quality control of the packaging materials.
A detailed study of the organisation and personnel involved in the pharmaceutical industry. These are involved in the guidelines of Good Manufacturing Practices.
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Document Maintenance in Pharmaceutical Industry.
By_ NAKUL DHORE
❖ Introduction
❖ Batch Formula Record
❖ Master Formula Record
❖ SOPs
❖ Quality Audit
❖ Quality Review & Quality Documentation
❖ Reports & Documents
❖ Distribution Records
❖ MCQs
Quality Assurance
As per B.PHARM 3rd Year Semester-6
(PCI Syllabus New)
Definition
Scope of calibration
Scope of validation
Frequency of calibration
Importance/ purpose of calibration
Importance/ advantages of validation
Difference between calibration & validation
QUALIFICATION & VALIDATION.Validation is an essential part of GMP, and an element of QA.Critical steps in the process need to be validated.Need for confidence that the product will consistently meet predetermined specifications and attributes.
Quality control on secondary packaging materialsAnupriyaNR
Presentation on quality control tests for the secondary packaging materials. Includes the materials used for secondary packaging, ideal properties of the secondary packaging material and various test procedures used for the quality control of the packaging materials.
A detailed study of the organisation and personnel involved in the pharmaceutical industry. These are involved in the guidelines of Good Manufacturing Practices.
The pharmaceutical Quality by Design (QbD) is a systematic approach to development that begins with predefined objectives and emphasizes product and process understanding and process control, based sound science and quality risk management.
Document Maintenance in Pharmaceutical IndustryNAKUL DHORE
Document Maintenance in Pharmaceutical Industry.
By_ NAKUL DHORE
❖ Introduction
❖ Batch Formula Record
❖ Master Formula Record
❖ SOPs
❖ Quality Audit
❖ Quality Review & Quality Documentation
❖ Reports & Documents
❖ Distribution Records
❖ MCQs
Quality Assurance
As per B.PHARM 3rd Year Semester-6
(PCI Syllabus New)
Definition
Scope of calibration
Scope of validation
Frequency of calibration
Importance/ purpose of calibration
Importance/ advantages of validation
Difference between calibration & validation
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I am uploading this GMP presentation to make aware who are working in pharma and help to maintain high standards in products manufacturing .
GMP Vs cGMP: It is my understanding that , Ultimately GMP & cGMP both the aim is same, means to prevention of the product from bad quality entering the market to endover peoples's life.
GMP applies to pharmaceutical and healthcare products and help to maintain high standards in these products.
cGMP is to remind accepting countries that all guidelines must be followed with latest and current production processes i.e employ technologies and systems which are up-to-date in order to comply with the regulation.
FDA (Food and Drug Administration) included the word “current” to ensure that regulated firms use the most current Good Manufacturing Practices (I believe that some firms would actually use outdated versions of the GMP’s to manufacture regulated products.
(the FDA have made their standards immediately identifiable i.e cGMP; Other international bodies such as the ICH, WHO use the term GMP, as do Canada, Japan and the EMEA (European authority). In FDA view cGMP means following 21 CFR 210 and 211 and no other.)
Presented By :- Raghav Sharma
Class :- M.Pharm, 1st sem.
Department :- Pharmaceutics
Institute :- Parul Institute of Pharmacy
Content :-
Current good manufacturing Practices
Equipment and their maintenance
Production Management
Conclusion
References
Pharmaceutical Validation: Role in Phamaceutical Industrykaunainfathema1
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[Note: This is a partial preview. To download this presentation, visit:
https://www.oeconsulting.com.sg/training-presentations]
Sustainability has become an increasingly critical topic as the world recognizes the need to protect our planet and its resources for future generations. Sustainability means meeting our current needs without compromising the ability of future generations to meet theirs. It involves long-term planning and consideration of the consequences of our actions. The goal is to create strategies that ensure the long-term viability of People, Planet, and Profit.
Leading companies such as Nike, Toyota, and Siemens are prioritizing sustainable innovation in their business models, setting an example for others to follow. In this Sustainability training presentation, you will learn key concepts, principles, and practices of sustainability applicable across industries. This training aims to create awareness and educate employees, senior executives, consultants, and other key stakeholders, including investors, policymakers, and supply chain partners, on the importance and implementation of sustainability.
LEARNING OBJECTIVES
1. Develop a comprehensive understanding of the fundamental principles and concepts that form the foundation of sustainability within corporate environments.
2. Explore the sustainability implementation model, focusing on effective measures and reporting strategies to track and communicate sustainability efforts.
3. Identify and define best practices and critical success factors essential for achieving sustainability goals within organizations.
CONTENTS
1. Introduction and Key Concepts of Sustainability
2. Principles and Practices of Sustainability
3. Measures and Reporting in Sustainability
4. Sustainability Implementation & Best Practices
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Editable Toolkit to help you reuse our content: 700 Powerpoint slides | 35 Excel sheets | 84 minutes of Video training
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www.seribangash.com
A Memorandum of Association (MOA) is a legal document that outlines the fundamental principles and objectives upon which a company operates. It serves as the company's charter or constitution and defines the scope of its activities. Here's a detailed note on the MOA:
Contents of Memorandum of Association:
Name Clause: This clause states the name of the company, which should end with words like "Limited" or "Ltd." for a public limited company and "Private Limited" or "Pvt. Ltd." for a private limited company.
https://seribangash.com/article-of-association-is-legal-doc-of-company/
Registered Office Clause: It specifies the location where the company's registered office is situated. This office is where all official communications and notices are sent.
Objective Clause: This clause delineates the main objectives for which the company is formed. It's important to define these objectives clearly, as the company cannot undertake activities beyond those mentioned in this clause.
www.seribangash.com
Liability Clause: It outlines the extent of liability of the company's members. In the case of companies limited by shares, the liability of members is limited to the amount unpaid on their shares. For companies limited by guarantee, members' liability is limited to the amount they undertake to contribute if the company is wound up.
https://seribangash.com/promotors-is-person-conceived-formation-company/
Capital Clause: This clause specifies the authorized capital of the company, i.e., the maximum amount of share capital the company is authorized to issue. It also mentions the division of this capital into shares and their respective nominal value.
Association Clause: It simply states that the subscribers wish to form a company and agree to become members of it, in accordance with the terms of the MOA.
Importance of Memorandum of Association:
Legal Requirement: The MOA is a legal requirement for the formation of a company. It must be filed with the Registrar of Companies during the incorporation process.
Constitutional Document: It serves as the company's constitutional document, defining its scope, powers, and limitations.
Protection of Members: It protects the interests of the company's members by clearly defining the objectives and limiting their liability.
External Communication: It provides clarity to external parties, such as investors, creditors, and regulatory authorities, regarding the company's objectives and powers.
https://seribangash.com/difference-public-and-private-company-law/
Binding Authority: The company and its members are bound by the provisions of the MOA. Any action taken beyond its scope may be considered ultra vires (beyond the powers) of the company and therefore void.
Amendment of MOA:
While the MOA lays down the company's fundamental principles, it is not entirely immutable. It can be amended, but only under specific circumstances and in compliance with legal procedures. Amendments typically require shareholder
Memorandum Of Association Constitution of Company.ppt
Euipment q a
1. A SEMINAR
ON
GMP - EQUIPMENT
1
Prepared By:
Nayan Jagani
M. Pharm Sem-1
Q.A . Department
Guided by:
Mr. Jignesh S. Shah
S. J. Thakkar Pharmacy College - Rajkot.
2. OVER VIEW FOR EQUIPMENT
Introduction
Equipment selection
Equipment design, size and location
Equipment construction
Equipment identification
Cleaning and maintenance
Automated, mechanical and electronic equipment
Filter
Weighing balance
Purchase specification
SOP
2
3. Introduction
Equipment may be defined as a physical entity which is used to
carry out a general or specific activity in the plant.
Equipment is the major inputs in the manufacture of the
pharmaceutical products, in the regulatory literature on GMP in
various countries gives the importance & hence provide
guidelines on the management of equipment in pharmaceutical
plants.
Equipment may be :
Single system or piece,
Integrated system.
3
4. Equipment Selection
Selection of equipment has both strategic and financial impact on the
companies.
It is an essential for any company because it has direct influence on the
success of the product facilities by optimum cost ,improving quality , safety
and reducing environmental hazards.
Factor that affect selection of equipment
a) Operating criteria,
b) Availability of spares and servicing
c) Maintenance,
d) Environmental issues,
e) Availability of design & maintenance manuals,
f) Cost.
4
5. Equipment
design, size and location
Equipment used in the manufacture, processing, packing or holding
of a drug product shall be of appropriate design, adequate size, and
suitably located to facilitate operations for its intended use.
Availability of design and maintenance manuals from the supplier
that are important for validation/qualification and maintenance
programs.
Equipment suitably located & designed for easy cleaning and
maintenance.
5
6. Equipment construction
Equipment shall be constructed so that surfaces that contact
components & drug products shall not be reactive or absorptive as it
alter the safety, identity, strength, quality or purity of the drug
product.
The construction material used for parts which are direct contact
with products & manufacturing vessels may be stainless steel 316 or
Borosilicate glass & tubing should be capable of being washed and
autoclaved.
Any substances required for operation such as lubricants or coolants
shall not come into contact with components, drug product
containers closures or drug products.
6
7. Equipment Identification
All compounding and storage containers, processing lines and
major equipment used during production of a batch of drug product
shall be properly identified at all times to indicate their content.
Major equipment shall be identified by a distinctive identification
no. or code that shall be recorded in the batch production record to
show the specific equipment used in the manufacture of each batch
of drug product.
7
8. Cleaning And Maintenance
Equipment and utensils shall be cleaned, maintained, and sanitized
at appropriate intervals to prevent contamination.
Written procedures shall be established and followed for cleaning
and maintenance of equipment, including utensils, used in the
manufacture, processing, packing, or holding of a drug product.
A cleaning procedure desired at end of working shift only for
equipment in which a wet processing stage has been carried out.
Cleaning and washing may be :
A. Manual
B. Automated
-CIP , -SIP
8
9. cleaning validation:-
why it is important?
Essential to establish adequate cleaning procedures.
Cleaning validation should be performed in order to confirm
the effectiveness of a cleaning procedure.
The data should support a conclusion that residues have
been reduced to an ‘acceptable’ level.
sampling methods:
Swab sampling,
Rinse fluid,
Placebo flush,
Visual Examination.
Analytical method:
HPLC, GC, HPTLC, pH , Conductivity, UV, ELISA.
9
10. Every equipment must have SOP’s for operation, cleaning and
maintenance. There may be system to distinguish equipment in
three categories:
Operational equipment ( with green card ),
Equipment under maintenance ( yellow card ),
Defective equipment (red card ).
The operator doing cleaning and maintenance must be so
trained that their activities of cleaning and maintenance will
not affect or contaminate product.
Records of all activities on equipment must be
chronologically recorded in the equipment log book.
10
11. Types of Maintenance
11
Equipment Maintenance: defined as facilities maintain to some desired
level of efficiency to keep assets in a satisfactory condition.
12. 12
Breakdown maintenance:-
It means that people waits until equipment fails and repair it. Such a thing could
be used when the equipment failure does not significantly affect the operation
or production or generate any significant loss other than repair cost.
Corrective maintenance ( 1957 ):-
It improves equipment and its components so that preventive maintenance can
be carried out reliably. Equipment with design weakness must be redesigned to
improve reliability or improving maintainability .
Maintenance prevention ( 1960 ):-
It indicates the design of a new equipment. Weakness of current machines are
sufficiently studied and are incorporated before commissioning a new
equipment.
13. 13
Preventive maintenance ( 1951 ) :-
It is a daily maintenance ( cleaning, inspection, oiling and re-tightening ),
design to retain the healthy condition of equipment and prevent failure through
the prevention of deterioration, periodic inspection or equipment condition
diagnosis, to measure deterioration. It is further divided into periodic
maintenance and predictive maintenance.
• Periodic maintenance ( Time based maintenance - TBM) :
Time based maintenance consists of periodically inspecting, servicing and
cleaning equipment and replacing parts to prevent sudden failure and process
problems.
• Predictive maintenance :-
This is a method in which the service life of important part is predicted based
on inspection or diagnosis, in order to use the parts to the limit of their service
life. Compared to periodic maintenance, predictive maintenance is condition
based maintenance.
14. SOP on cleaning, operation and maintenance
Name of equipment and its unique identification no.
Responsible person to carry out and supervise operation
schedule maintenance and cleaning.
Material use for cleaning and its complete removal after cleaning.
Removal of previous batch identification.
Protection of cleaned equipment.
Inspection of cleaned equipment.
Detailed step by step operation of equipment.
Detailed step by step prcedure to carry out prevententive maintenance.
Record of cleanig, maintenance and operation.
14
15. Department : Month:
Equipment: Make:
Equipment identification No.: Working Capacity:
Cleaning sop no.: Maintenance sop no.:
Cleaning Maintenance
Date Sign Remark Date Sign Remark
Equipment cleaning & maintenance record
15
16. INDIAN PHARMACEUTICAL LTD.
Daily maintenance record sheet
Sr. no. Department Work
performed
Time Part
replacedStarting completion
Date:________
Work left for next day:______________________________________
________________________________________________________
Remark:_________________________________________________
Work performed by Inspected by Deptt. Head
________________________________________________________
________________________________________________________
16
17. INDIAN PHARMACEUTICAL LTD.
Machine breakdown card
Name Of Machine: Room No.:
Identification No.:
Department:
17
Sr.
No.
Date Time Type of
breakdown
Maintenance work
performed
Time Sign
Part
Name/Part
No.
Replace From To
18. USP divides the equipment into three groups based
on respective complexity
Group A Group B Group C
•E.g. stirrer •E.g. pH meter,
balance
E.g. HPLC,GC
•They are
simplest.
•Only visual
observation is
needed to
confirm that it is
qualified.
•Little complex.
•Written procedure
must be followed.
•Though testing of
their qualification is
generally
straightforward and
identifiable.
•Highest complex.
•Deep n complete
literature must be
provided.
18
20. These types of equipment includes computers or related
systems that will perform a function satisfactorily, may
be used in the manufacture, processing, packing, and
holding of a drug product. It should be routinely
calibrated, inspected or checked according to a written
program designed to assure proper performance.
Written records of those calibration checks and
inspections shall be maintained.
20
AUTOMATIC, MECHANICALAND ELECTRONIC
EQUIPMENT
21. Appropriate controls shall be exercised over computer or related system
to assure that changes in master production and control records or other
records are instituted only by authorized personnel.
Input and output from the computer or related system of formulas or
other records or data shall be checked for accuracy.
The degree and frequency of input/output verification shall be based on
the complexity and reliability of the computer or related system
A backup file of data entered into the computer or related system shall
be maintained except where certain data, such as calculations performed
in connection with laboratory analysis, are eliminated by computerization
or other automated processes. In such instances a written record of the
program shall be maintained along with appropriate validation data.
21
22. Filters
Filter used as a part of equipment & Filtration is one of the processes use in
pharmaceutical operation and air systems.
Filter for liquid filtration used in the manufacture, processing or packing of
injectable drug products intended for human use shall not release fiber into
products.
As a part of GMP, filters should be considered from following:
Type of filter and filration process,
Compatibility of filter media with processing material,
Cleaning of reusable filter and their sanitization,
validation of filter,
Disposal of filter.
22
23. INDIAN PHARMACEUTICAL LTD.
Pre-air filter record
Sr.
no.
location Cleaning
date
Clean by Manometer
reading
before
Manometer
reading after
washing
Rema
rk
water Air
1
2
3
4
5
Name of filter:
Size:
Pore size:
23
24. Weighing balance
Balance and other measuring equipment of appropriate range and precision
should be available for production and control operation.
Measuring, weighing, recording and control equipment should be calibrated
& checked at defined interval by appropriate method. Adequate record of such
tests should be maintained.
All weighing balance should be in a state of calibration. The name, signature
and date of person weighing and supervising weighing operations must be
recorded.
A list of various weighing balance should be made with following:
Description of balance ,
Model number,
Weighing range,
location,
Frequency of calibration.
24
25. Purchase specification of equipment
Definition:- Detailed description of the measurable characteristics
desired in an equipment to be purchased such as quality, size,
weight , performance parameters, safety requirements etc.
The documents used for the procurement of equipment should
consist:
User Requirement Specification
Relevant Standard Demand Specifications, and
Purchase Agreement.
25
26. Purchase specification of UV-VIS Spectrophotometer, double beam
Wavelength : 190-900 nm or more
Optical System : Double beam with double monochromator
Light Source : D2 and Tungsten
Wavelength accuracy : +/- 0.1 nm
Spectral Bandwidth : at least, 0.5, 1, 2, 5 (variable)
Photometric Range : at least -0.3~3 Abs
Photometric Modes : Abs,%T
Stray Light minimum
Wavelength Scan Speed : 800-10 nm/min
Baseline Stability : +/-0.0008Abs/Hour or less
Detector : Photomultiplier R928
Control : By Computer
Quartz Cuvette
Branded Computer monitor with latest specification
Laser Printer
D2 Lamp, tungsten Lamp
5 years maintenance of the system
26
27. Purchase specification of water bath
10 L to 15 L water tank volume
Water circulation to maintain uniform temperature
Working temperature : ambient +5˚C to 100˚C or more
Stability : ±0.1˚C or less
Increment : ±1˚C or less
Microprocessor control for precise temperature
Over-temperature cut-off
Audible and visible alarms
LED display with 0.1˚C resolution for temperature
Operable at 220 volts
5 year equipment maintenance
27
28. SOP for Equipment
Definition: A written authorized procedure which gives instructions for
performing operations necessarily specific to a given equipment.
What are SOPs ?
They are the tools to ensure that GMP is being followed wherever
applicable.
It contains relevant information about any activity or process carried
out (like calibration validation , maintenances , cleaning , production ,
packing or even for receipt or movement of raw material ).
Why SOPs are needed?
Due to demand of safe and efficacious drug product in the market.
In addition to clinical factors storage , handling of raw material and
final product , cross contamination and batch to batch deviation
affects the quality of product.
We don’t want any loss or refusal.
28
29. 29
Precautions for preparing SOPs:-
Information & procedures in clear and unambiguous language and
specifications for the facilities should be provided.
By following SOPs the quality product should be expected.
Significant deviations are recorded and investigated.
Documents must not be changed or added or reviewed or amended without any
authorization.
Easy to retrieve from master SOP and check also critical steps should be
highlighted.
Must not allow any error.
Regularly updated and previous suspended SOPs are preserved for at least 1
year after the last batch made on it has been expired.
Original copy is kept in locker and one copy is displayed in all the concern
areas and retained with each member who has signed in it.
30. GOOD QUALITY PHARMACEUTICALS PVT. LTD.
STANDARD OPERATING PROCEDURE
Name of equipment:-
Model No.:-
Purpose:-
Scope:-
Responsibility:-
Procedure:-
Prepared By
(GM Production)
Checked By
(QC Manager)
Authorized By
(DirectorTechnical)
30
Department : Procedure no.: Page no. : _ to_
Effective Date : Superceeds earlier procedure date : Review date :
32. INDIAN PHARMACEUTICALS LTD.
List of equipment
Sr. No. Name of
Equipment
Capacity
Output/Holding
Make Date Of
Installation
Material of
Construction
32
33. Laboratory Master File of Instruments
Instrument
Name
Manufac
turer
Maintenance
Frequency
Service &
Repair
conducted
by:
Calibration
Frequency
Calibration procedure
33
34. Reference:
C-Gmp for pharmaceutical by Manohar A. Potdar
Quality Manual, by D. H. Shah
Good Manufacturing Practices for Pharmaceuticals, vol. 109 ,
Marcel Dekkar Inc., N. Y.
www.wikipedia.com
www.pharmaquality.com
34