Blend Uniformity - PQRI Research

Slides:



Advertisements
Similar presentations
ICH Q4B Regulatory Acceptance of Analytical Procedures and/or Acceptance Criteria (RAAPAC) Overview and Update Robert H. King, Sr. Office of Pharmaceutical.
Advertisements

Statistical Evaluation of Dissolution for Specification Setting and Stability Studies Fasheng Li Associate Director, Pharmaceutical Statistics Worldwide.
Statistical Approaches to Addressing the Requirements of the New FDA Process Validation Guidance for Small Molecules 1 Jason Marlin, MS/T Statistics, Eli.
Methods of tablet manufacturing
Manufacturing Process
Week # 12 MR Chapters 11 & 12 Tutorial #12 MR #11.2, 12.1.
Determine impurity level in relevant batches1
Office of New Drug Chemistry, OPS, CDER, Food and Drug Administration Establishing Dissolution Specification Current CMC Practice Vibhakar Shah, Ph.D.
Slide 1 of 19D.K. Mubangizi, Dar Es Salaam Sept Training Workshop for Evaluators from National Medicines Regulatory Authorities in East African Community.
COMPARABILITY PROTOCOLS ACPS March 12-13, 2003 Stephen K. Moore, Ph.D. Chemistry Team Leader CDER/Office of New Drug Chemistry Co-Chair, Comparability.
Assessing Quality-by-Design A CMC Review Perspective
Emerging Science Issues in Pharmaceutical Manufacturing: Process Analytical Technologies Ajaz S. Hussain, Ph.D. Office of Pharmaceutical Science CDER,
Regulatory requirements on Medicine Stability Guidelines relevant for Stability testing Sultan Ghani.
World Health Organization
Challenges and Opportunities in Enhancement of the CMC Section of NDAs: Quality – by - Design Ajaz S. Hussain, Ph.D. Deputy Director Office of Pharmaceutical.
Introduction Background to the work of the BUWG Garth Boehm
PAT Validation Working Group Process and Analytical Validation Working Group Arthur H. Kibbe, Ph.D. Chair June 13, 2002.
1 ACPS November 15, Update Nancy B. Sager, Associate Director Office of Pharmaceutical Science Center for Drug Evaluation & Research Food and.
FDA Nasal BA/BE Guidance Overview
A Seminar on 1.  Why to validate?  Parts of Equipment Validation  Who should do Equipment Validation?  Equipment qualification  Typical process flow.
Ensuring Physical Stability of Pharmaceuticals: Can/should we improve our ability to identify and prevent physical changes? Ajaz S. Hussain, Ph.D. Deputy.
Validation of Analytical Method
Achieving and Demonstrating “Quality-by-Design” with Respect to Drug Release/dissolution Performance for Conventional or Immediate Release Solid Oral Dosage.
Organizational Gaps in Reaching the “Desired State” Helen Winkle.
Nonclinical Studies Subcommittee Advisory Committee for Pharmaceutical Science CMC Issues for Screening INDs Eric B. Sheinin, Ph.D. Acting Deputy Director.
ITFG/IPAC Collaboration CMC Specifications Technical Team ITFG/IPAC TECHNICAL TEAM: CMC SPECIFICATIONS Presented by: Bo Olsson, PhD 26 April 2000 Rockville,
Inspection Issues in the Analytical Laboratory: An FDA Perspective Yvonne McKnight Chemist US Food and Drug AdministrationPhone: x
ACPS Advisory Committee Meeting October , 2002 ACPS Advisory Committee Meeting October , 2002 Scientific Considerations of Polymorphism in.
Moving Towards the “Desired State”: Scientific Gap Analysis Ajaz S. Hussain, Ph.D. Deputy Director, Office of Pharmaceutical Science, CDER, FDA 20 October.
Chapter 1 Introduction to Chemistry
Flow Behavior of Granular Materials and Powders Part II
Ajaz S. Hussain, Ph.D. Deputy Director Office of Pharmaceutical Science, CDER, FDA ACPS Subcommittee on Manufacturing Science: Identification and Prioritization.
2015 MBSW1 Quality Assurance Test of Delivered Dose Uniformity of Multi-dose Spray and Inhalation Drug Products Drs. Yi Tsong 1, Xiaoyu (Cassie) Dong*
FDA Regulation of Drug Quality: New Challenges Janet Woodcock, M.D. Director, Center for Drug Evaluation and Research, Food and Drug Administration April.
1-7.The ICH Q8 “Minimal Approach” to Pharmaceutical Development
Important informations
1 Regulatory Aspects of Pharmaceutical Excipients PQRI Workshop Nick Buhay Acting Director Division of Manufacturing and Product Quality Office of Compliance.
Bioequivalence Studies and Other Recommendations for Orally Inhaled and Nasal Drug Products: Work of the ITFG/IPAC-RS Collaboration Presented by Cynthia.
Predicting Physical Stability in Q1A(R) Chi-wan Chen, Ph.D. Office of New Drug Chemistry Center for Drug Evaluation and Research Food and Drug Administration.
Overview of FDA's Regulatory Framework for PET Drugs
Critical Material Properties for Pharmaceutical Dosage Forms - Industry Perspective Tony Hlinak Abbott Laboratories North Chicago, IL.
1 Basis of the Proposed Tactical Plan for a QbD approach for Quality Control and Assurance of Dissolution Rate Ajaz S. Hussain, Ph.D. Deputy Director,
The USP Performance Test Dissolution Systems Suitability Studies Walter W. Hauck, Ph.D. USP Consultant Presentation to Advisory Committee for Pharmaceutical.
COMPARABILITY PROTOCOLUPDATE ADVISORY COMMITTEE FOR PHARMACEUTICAL SCIENCE Manufacturing Subcommittee July 20-21, 2004 Stephen Moore, Ph.D. Chemistry Team.
Purdue University – Industrial and Physical Pharmacy - Morris Discussion Questions of Polymorphism in ANDAs Ken Morris Industrial and Physical Pharmacy.
Satish Mallya January 20-22, |1 | 2-3. Pharmaceutical Development Satish Mallya Quality Workshop, Copenhagen May 18-21, 2014 May 18-21,2014.
Properties, Handling and Mixing of Particulate Solids By Sidra Jabeen Department of Chemical Engineering, University of Engineering & Technology Lahore.
Blend Uniformity: Update Ajaz S. Hussain, Ph.D.. Background Issue: Assuring and documenting “adequacy of mixing” operations –PQRI’s Proposal Stratified.
Validation Defination Establishing documentary evidence which provides a high degree of assurance that specification process will consistently produce.
1 Office of Pharmaceutical Science on Jon Clark FDA/CDER/OPS Associate Director for Policy Development.
1 PAT Subcommittee Closing Report 12 March 2003 Tom Layloff Acting Chair.
Second Meeting of the FDA/ACPS Process Analytical Technology: Closing Remarks Ajaz S. Hussain, Ph.D. Deputy Director Office of Pharmaceutical Sciences.
Pharmaceutical Quality Control & current Good Manufacturing Practice
Lawrence X. Yu, Ph.D. Director for Science Office of Generic Drugs, OPS, CDER, FDA ACPS Meeting, ACPS Meeting, Oct. 22, 2003 Office of Generic Drugs Research.
SEMINAR ON PRESENTED BY BRAHMABHATT BANSARI K. M. PHARM PART DEPARTMENT OF PHARMACEUTICS AND PHARMACEUTICAL TECHNOLGY L. M. COLLEGE OF PHARMACY.
Ajaz S. Hussain, Ph.D. Office of Pharmaceutical Sciences CDER, FDA October 21, 2003 Dose Content Uniformity: Parametric Tolerance Interval Approach.
Chemical Engineering Department Government Engineering College
Office of Pharmaceutical Science OPS Center for Drug Evaluation and Research CDER FDA Food and Drug Administration HHS Health and Human Services 1 Advisory.
HOLD-TIME STUDIES.
FLOW PROPERTIES OF SOLIDS
Pharmaceutical Quality Control & current Good Manufacturing Practice
EPA Method Equivalency
Evaluation of tablet Lab 5.
Evaluation of tablet Lab 5.
Chemical Engineering Explained
Mixing Lab 7.
Flow properties of pharmaceutical particles
Evaluation of tablet Lab 5.
Quality guidelines on impurities
SID & GP MINPROMTORG OF RUSSIA Corporate Communication Center
Presentation transcript:

Blend Uniformity - PQRI Research Ajaz S. Hussain, Ph.D. Deputy Director Office of Pharmaceutical Science CDER, FDA

Background Blend uniformity analysis (BUA) S. Sonja Sekulic Pfizer Groton Laboratories Background Blend uniformity analysis (BUA) a in-process test Subject of intense debate (~10 years) Sample size (1-3x,..), sampling errors, segregation following blending, lack of correlation with content uniformity,…. CGMP issue vs. review issue Inconsistent enforcement Draft ANDA Guidance - August 1999 PQRI BUA Project

Draft Blend Uniformity Guidance ‘99 Motivation Inconsistency with respect to supplements for deleting BUA Concern regarding drug content uniformity Insufficient information to ensure that “quality was by design” Blender type, capacity, operating speed and blending time (generally same for pilot and proposed commercial batch) Recommendations Scope - for products which require USP content uniformity testing For complex dosage forms - consult the review div. Not to submit a supplement to delete BUA when it is also used for compliance with CGMP Sampling size and procedure Acceptance criteria and analytical procedure

Unconfined yield stress Performance of a Solids Processing Units AIChE Journal 47: 107-125 (2001) Performance of a Unit Bulk Mechanical Properties Angle of repose Unconfined yield stress Forces Acting on Particles Adhesion forces Impact forces Material Characteristics Hamaker constant Dielectric constant Young’s modulus Particle Attributes PSD Shape Composition Equipment Design Geometry Constituent parts Material properties Operating Conditions Speed of moving parts Temperature Humidity

Today Trial-Error is the Norm Do SOP’s reflect established Heuristic rules? Segregation is not a serious problem if all the particles are smaller than 30 um or if they are slightly moist Establish acceptance criteria for particle size distribution of excipients Avoid bulk solids transfer where particles slide down a long, inclined chute Segregation due to percolation is likely to be a concern if the particles of different density or size are poured into a heap or let slide on an inclined chute The tendency of segregation of binary mixtures due to percolation decreases substantially if the ratio of particle diameters is lower than 1.3 Segregation during emptying of a storage unit is accentuated when funnel flow occurs Ensure mass flow in hoppers AIChE Journal 47: 107-125 (2001)

USP Content Uniformity A question of “representative sample”? PQRI Proposed Stratified Sampling Blend Sample Analysis (Thief) %RSD = <1 PASS USP Content Uniformity Stage 1: PASS

Questions Is the current PQRI proposal appropriate for inclusion in a planned revised guidance? If no, please suggest modifications or improvements. If yes, should the proposed stratified sampling and analysis plan be applicable only for the bioequivalence batch and validation batches?

Question (Contd.) If the proposed stratified sampling and analysis plan is limited only to bioequivalence and validation batches, how should adequacy of mix be ensured for routine production batches?