Regulatory affairs-Introduction to CTD
-
Upload
mahesh-shinde -
Category
Healthcare
-
view
11.434 -
download
12
Transcript of Regulatory affairs-Introduction to CTD
05/02/23 1
Drug Regulatory Affairs
By, Mahesh Shinde
The Bridge BetweenPharma Companies &
Govt. Agency
2
Regulatory affairs
• It is by no means boring! It’s interesting.
3
Role of Regulatory Affairs
What is this?
4
Regulatory System
YES YES YES
YES
YES
YES
Govt. Prescriber Distributor Patient
Govt.
Prescriber
Distributor
Patient
5
• Drug = medicinal product = pharmaceutical product
6
Drug regulatory affairsAny activity with drugs
By whom? (the authority)
no (=does not belong to drug regulatory affairs)
yes
Prior authorisation needed?
Based on which (objective and subjective) criteria?
Subject to regular control (quality, inspection)?
By whom? (the authority)Based on which (objective and subjective) criteria?
7
Activities with drugs…
• research (chemical, biological)• clinical trials on human beings• manufacture• registration
– evaluation– authorisation
• (wholesale) distribution
continued
8
Activities with drugs (cont’d)
• pricing• prescribing• reimbursement/subsidy• advertising (if any)• special control (e.g. narcotics)• post-marketing surveillance
– national drug quality control lab– adverse effect reporting system
• (retail) distribution• etc.
poppy
Quality = Quality of Personnel (Qualification, Training…) + Quality of Materials (Specifications, Approved
Suppliers...) + Quality of Means (Qualified equipment's,
maintenance…) + Quality of Media (GMP premises, Controlled
environment…)
+ Quality of Methods (Calibration, Validation…)
Composition of Quality
9
QUALITYQUALITYRaw Materials
Personnel
Procedures
Validated processes
EquipmentPremises
Environment
Packing Materials
Functions of a Quality Unit
10
Quality Control– Sampling and testing of components
Raw materials, Packing materials, intermediates and finished products
– Compliance to Good Laboratory Practices (GLPs)
Functions of a Quality Unit
11
Quality Assurance– Designing robust quality
systems
– Ensure compliance to relevant regulatory requirements
– Ensure compliance to requirements of Good Manufacturing Practices (GMP)
Value addition in QA Value addition in QA functionfunction
12
Quality Assurance:– Perform structured self-
inspection audits at regular intervals to prevent any failure or non-conformance
– Critically analyze the quality non-conformance issues and suggest corrective and preventive actions
Value addition in QA function
13
Quality Assurance:– Perform documentation
audit to ensure realistic recording of all the relevant process parameters
– Review the adequacy of in-process control checks to prevent any potential failures
Value addition in QA function
14
Quality Assurance:– Training & Knowledge
Management
– Perform literature survey of FDA / ICH / ISO guidelines, revisions in the Pharmacopoeial specifications and the current regulatory requirements and provide training to the production personnel.
What is Dossier?
15
• Dossier is collection or file of documents that contains all the technical data of pharmaceutical product to be approved/ registered /marketed in country.
• It is commonly called as registration dossier.
In US : New Drug ApplicationIn EU : Marketing Authorization Application
What is DMF?Drug Master File (DMF)
• US : United State Drug Master File (US-DMF)• EU : European Drug Master File (EDMF) or Active Substance Master File (ASMF)
• TYPES OF DMFs• The types of DMFs are:• Type I - Manufacturing Site, Facilities, Operating Procedures, and Personnel
(no longer applicable)• Type II - Drug Substance, Drug Substance Intermediate, and Material Used in Their Preparation, or Drug Product• Type III - Packaging Material• Type IV - Excipient, Colorant, Flavor, Essence, or Material Used in Their Preparation• Type V - FDA Accepted Reference Information
16
What is CTD/eCTD?Common Technical Documents (CTD)
• The Common Technical Document (CTD) is a set of specification for application dossier for the registration of Medicines and designed to be used across Europe, United States & ROW.
• Its electronic version called as Electronic Common Technical Document (eCTD)
17
The CTD Triangle
18
Module 1 Administrative & Prescribing Information (Region Specific):
Should Contain Documents specific to each region:
19
Module 1 Administrative & Prescribing Information (Region Specific):
(1) SITE MASTER PLAN OF PLANT(2) COMPANY PROFILE IN SHORT(3) ATTESTED COPY OF MANUFACTURING LICENCE(4) ATTESTED COPY OF PRODUCT PERMISSION FROM FDA(5) ATTESTED COPY OF COPP(6) ATTESTED COPY OF WHO/GMP CERTIFICATE(7) COA OF SAMPLE(8) ATTESTED COPY OF WHOLE SELL LICENCE.(9) LETTER OF AUTHORISATION
20
Module 2 CTD Summaries (QOS):
21
It contain 7 sections in the following order: 2.1 CTD Table of content (Module 2-5)2.2 CTD Introduction2.3 Quality Overall Summary
2.4 Non-Clinical Overview
2.5 Clinical Overview
2.6 Non-Clinical Summary
2.7 Clinical Summary
Module 3 Quality: Chemistry, Manufacturing & Controls (CMC)
22
3.1 Table of content (Module 3)3.2 Body of Data
3.2 S Drug Substance 3.2 S1 General Information (Name, Mfg.) 3.2 S2 Manufacture
3.2 S3 Characterization 3.2 S4 Control of Drug Substance (Specification, Analytical procedures, Validation of Analytical procedures, etc. )
3.2 S5 Reference Standards
3.2 S6 Stability
Module 3 Quality: Chemistry, Manufacturing & Controls (CMC)
23
3.2 P Drug Product 3.2 P1 Description and Composition of the Drug Product3.2 P2 Pharmaceutical Development (name, dosage form)3.2 P3 Manufacturer
3.2 P4 Control of Excipients
3.2 P5 Control of Drug Product (Specification, Analytical procedures, Validation of Analytical procedures, etc. )
3.2 P6 Reference Standards
3.2 P7 Stability
Module 3 Quality: Chemistry, Manufacturing & Controls (CMC)
24
3.2 A Appendices3.2 A1 Facility & Equipment's
3.2 A2 Advertising agents safety evaluation
3.2 A3 Excipients
3.2 R Regional Information
3.3 Literature References
Module 4 Non-Clinical Study Reports:
25
4.1 Table of content (Module 4)4.2 Study Reports
4.2.1 Pharmacology4.2.1. 1. Pharmacodynamics 4.2.1. 2. Safety Pharmacology 4.2.1. 3. Pharmacodynamics Drug Interaction
4.2.2 Pharmacokinetics4.2.2. 1. ADME 4.2.2. 2. Pharmacokinetic Drug Interaction 4.2.2. 3. Other Pharmacokinetic Study
Module 4 Non-Clinical Study Reports:
26
4.2.3 Toxicology4.2.3. 1. Single/Repeat Dose Toxicity 4.2.3. 2. Genotoxicity
4.2.3. 3. In-Vivo/Vitro Toxicity
4.2.3. 4. Carcinogenicity 4.2.3. 5. Local Tolerance/Dependence 4.2.3. 6. Other Studies
4.3 Literature References
Module 5 Clinical Study Reports:
27
5.1 Table of content (Module 5)5.2 Tabular listing of Clinical Studies 5.3 Clinical study reports
5.3.1 Reports of Biopharmaceutical (BA-BE) Study 5.3.2 Reports of Pharmacokinetic (biomaterial) study 5.3.3 Reports of Pharmacokinetic (PK) studies 5.3.4 Reports of Pharmacodynamics (PD) studies 5.3.4 Reports of Efficacy and Safety studies 5.3.4 Reports of Post-Marketing experience 5.3.4 Case Report Forms & Individual patient listings
5.4 Literature References
Sample
• Dossier • DMF
Regulatory Compliance
National Regional Global
Regulatory Compliance
29
National (India)
License Application Receipt
Manufacturing license Form No. 24 Form No. 25
Test license Form No. 30 Form No. 29
Import license Form No. 12 Form No.11
30
Compliance to (Drugs & Cosmetics Act 1940 & Rules under)
National (India)
Drug Regulatory approval
Schedule Y ComplianceForm 44
Manufacturing Schedule M Compliance
Documentation Schedule U Compliance
Packaging Schedule P Compliance
API/Excipients/FP/PM IP Inputs if not BP/USP/ or IH
31
Regulatory Dossier Regulatory approach:
Parameters US Europe Other markets India
API USP Ph.Eur. USP / Ph.Eur. IP
USDMF COS (CEP) / EDMF DMF requirement depends on the target market
Excipients USP Ph.Eur. USP / Ph.Eur. IP
Reference product US Europe Depends on the target market
Indian (if not available, then US or Europe)
Packaging materials
Complying to USP Ph.Eur. USP / Ph.Eur. IP
Finished product USP As per Ph.Eur. General requirement
USP / Ph.Eur. IP
Submission batch 1 2 2 or 3 -
Submission batch size
100,000 units or 1/10th of commercial
batch
100,000 units or 1/10th of
commercial batch
Depends on the target market
No such requirement
32
Regulatory Dossier Regulatory approach:
Parameters US Europe Other markets India
Stability data 1 batch 2 batches 2 or 3 batches 3 batches
Stability condition Zone I & II condition Zone I & II condition Depends on the target market
Zone IV condition
Comparative dissolution study
3 media 3 media Depends on the target market
1 to 3 media
Input materials TSE/BSE, OVI statements
TSE/BSE Depends on the target market
No such requirement
Packaging materials Food grade certificate Food grade certificate Depends on the target market
No such requirement
Method validation data As per ICH ICH ICH No such guideline
Process validation data
Not required Not required Depends on the target market
Not required for submission
Bioequivalence study US reference product under fast and fed
condition
European reference product (generally
under fasting condition)
Generally fasting bio study
Fasting bio study
Bioequivalence study In USFDA approved CRO anywhere in the
world
MHRA/EU approved CRO anywhere
Depends on the target market
Indian study required
33
Regulatory Authorities India: DCGI & State Drug Administration European Union: MHRA USA : Food and Drug Administration (FDA) Australia : Therapeutic Goods Administration Newzeland : Medsafe South Africa: Medicines council control Japan : Ministry of Health & Labour Welfare Switzerland : Swissmedic Brazil : ANVISA (The National Health Surveillance Agency) Mexico: COFEPRIS (The Federal Commission for the Protection against Sanitary Risk) Chile : ISP - Instituto de Salud Pública de Chile Columbia: INVIMA – Instituto Nacional de Vigilancia de Medicamentos Alimentos Carrera 68 D No. 17 - 11 / 21 Argentina: ANMAT - set in 1992 Argentine National Administration of Drugs, Food & Medical TechnologyFrance: Agence Française de Sécurité Sanitaire des Produits de SantéGermany: Federal Institute for Drugs and Medical Devices
34
Important sitesRegulatory sites:
www.fda.govwww.tga.gov.au http://www.emea.europa.eu/ www.ministeriodesalud.go.cr www.mspas.gob.gthttp://www.minsa.gob.pa/minsa2006/inicio.phphttp://www.minsa.gob.nihttp://www.salud.gob.hn/www.cssp.gob.svhttp://www.sns.gov.bo/http://www.inh.gov.ec/http://www.mspbs.gov.py/http://www.msp.gub.uy/index_1.htmlhttp://digemid.minsa.gob.pehttp://www.inhrr.gov.vehttp://pharmacos.eudra.org
35
Important sitesUseful links:
•www.usp.org •www.pheur.org •www.jpdb.nihs.go.jp •www.picscheme.org •www.pda.org •www.phrma.org •www.pharmacy.org •www.elsevier.com •www.ich.org•www.ijpsonline.com •www.pharmj.com •www.scripnews.com
36
E-mail: [email protected]
37