Rx-360 Supplier Assessment Questionnaire (SAQ)



Similar documents
Quality Agreement. by and between. Supplier Name. Address: and. Client Name: Address:

Questionnaire Layout:

Quality Information. Buchs Manufacturing Site

ICH guideline Q7 on good manufacturing practice for active pharmaceutical ingredients questions and answers

MeriCal Quality Profile

Q7 Implementation Working Group ICH Q7 Guideline: Good Manufacturing Practice Guide for Active Pharmaceutical Ingredients Questions and Answers

Auditing as a Component of a Pharmaceutical Quality System

Library Guide: Pharmaceutical GMPs

The purpose of this Supplier Quality Standard is to communicate the expectations and requirements of Baxter Healthcare Corporation to its suppliers.

Quality Agreement Template

FOOD SAFETY MANAGEMENT SYSTEMS (FSMS): REQUIREMENTS FOR ANY ORGANISATION IN THE FOOD CHAIN (ISO 22000:2005)

NSF Dietary Supplement

GOOD MANUFACTURING PRACTICE GUIDE FOR ACTIVE PHARMACEUTICAL INGREDIENTS

INTERNATIONAL CONFERENCE ON HARMONISATION OF TECHNICAL REQUIREMENTS FOR REGISTRATION OF PHARMACEUTICALS FOR HUMAN USE

Revision Date Author Description of change Jun13 Mark Benton Removed Admin. Manager from approval

EUROPEAN COMMISSION HEALTH AND CONSUMERS DIRECTORATE-GENERAL. EudraLex The Rules Governing Medicinal Products in the European Union

Audit Report in the framework of the APIC Audit Programme

COMPLIANCE BY DESIGN FOR PHARMACEUTICAL QUALITY CONTROL LABORATORIES INSIGHT FROM FDA WARNING LETTERS

Optimizing Quality Control / Quality Assurance Agents of a Global Sourcing / Procurement Strategy

1. Scope This SOP covers requirements for PHARMCO-AAPER s Quality Management System

RTP s NUCLEAR QUALITY ASSURANCE PROGRAM

Checklist. Standard for Medical Laboratory

Good Manufacturing Practices (GMP) for Pharmaceutical Excipients

Quality Management System (QMS) for Active Pharmaceutical Ingredients (API) Manufacturers

ONTIC UK SUPPLIER QUALITY SURVEY

Pharmaceutical Wholesaler Site Inspection Checklist

ORACLE PROCESS MANUFACTURING QUALITY MANAGEMENT

International GMP Requirements for Quality Control Laboratories and Recomendations for Implementation

ASSESSMENT OF QUALITY RISK MANAGEMENT IMPLEMENTATION

Annex 9 Guide to good storage practices for pharmaceuticals 1

Audits must be conducted with due concern for employee safety and environmental protection.

Guidance for Industry: Starting Material Supplier Management

Community Guide to Good Practice For Feed Additive and Premixture Operators

Food Safety and Quality Management System

GLUTEN-FREE CERTIFICATION PROGRAM

Quality Management System MANUAL. SDIX, LLC Headquarters: 111 Pencader Drive Newark, Delaware 19702

Quality Management System MANUAL. SDIX, LLC Headquarters: 111 Pencader Drive Newark, Delaware 19702

PROPOSED UPDATED TEXT FOR WHO GOOD MANUFACTURING PRACTICES FOR PHARMACEUTICAL PRODUCTS: MAIN PRINCIPLES (JANUARY 2013)

Annex 2. WHO good manufacturing practices for pharmaceutical products: main principles 1

SQF SYSTEMS PRACTICE TEST / OCTOBER, 2012 American Food Safety Services Division, Technical and Business Services, LLC

Comparison between FDA QSR and ISO 13485

Welcome Computer System Validation Training Delivered to FDA. ISPE Boston Area Chapter February 20, 2014

ICH guideline Q10 on pharmaceutical quality system

BRC Food Safety and Quality Management System. New Issue 7

IFS Food Safety and Quality Management System

LIBRARY GUIDE. Online Courses. March 2012

MSC Group Chain of Custody (CoC) Guidance for Non-Reduced Risk Groups

PHARMACEUTICAL QUALITY SYSTEM Q10

UNICEF s Quality Assurance System for Procurement of Micronutrient Powders (MNP)

NSF International Standard / American National Standard. NSF/IPEC/ANSI Good Manufacturing Practices (GMP) for Pharmaceutical Excipients

Recent Updates on European Requirements and what QPs are expected to do

USP Pharmaceutical Ingredient Supplier Qualification Program. Manual for Participants

Testing Automated Manufacturing Processes

A Natural Products Association Presents. SQF Certification. Josh Grauso Technical Sales Director UL Registrar

Quality Manual PA

Guidance for Industry Quality Systems Approach to Pharmaceutical CGMP Regulations

Hazard Analysis and Critical Control Points (HACCP) 1 Overview

FSSC Certification scheme for food safety systems in compliance with ISO 22000: 2005 and technical specifications for sector PRPs PART II

Leila Kakko Tampere University of Applied science TRADITIONAL FOOD IN COMBATING FOODBORNE PATHOGENS 2011

Comparative analysis between the possible regulatory approaches to GMP compliance TITOLO PRESENTAZIONE

Annex 7 Guidelines on pre-approval inspections

CONCEPTS OF FOOD SAFETY QUALITY MANAGEMENT SYSTEMS. Mrs. Malini Rajendran

ICH Q10 Pharmaceutical Quality System (PQS)

ISO 13485:201x What is in the new standard?

FAMI-QS Certification Rules for Operators. Rules for Operators

Quality Management System General

Supplier Quality Agreements

Preparing for the Pre-Approval Inspection What to do Before the FDA Arrives. Barry A. Friedman, Ph.D. Consultant

Commercial Manufacturing - Qualification & Validation-related GMP Deficiencies and Other Lifecycle Considerations

SUPPLIER QUALITY SELF AUDIT & QUESTIONNAIRE FORM

CONTROL PLANS IN FOOD SAFETY MANAGEMENT SYSTEMS

GRADUATE CERTIFICATE IN GOOD MANUFACTURING PRACTICE (GMP) Plan your career for tomorrow and you will be ahead of your competitors

European Guide to good practice for the industrial manufacture of safe feed materials

Guidance for Industry. Q10 Pharmaceutical Quality System

ISO Food Safety Management System

This interpretation of the revised Annex

Example of a food company quality

Quality Management System for Active pharmaceutical Ingredients manufacturers. Integrating GMP into ISO 9001

Schweppes Australia Head Office Level 5, 111 Cecil Street South Melbourne Victoria

Addressing Risk in Partner / Contractor Selection and Onboarding. Michael Davidson VP Quality Systems and Compliance March 2014

AS9100 Quality Manual

Calibration & Preventative Maintenance. Sally Wolfgang Manager, Quality Operations Merck & Co., Inc.

Contents 1.0 FROM THE CHIEF EXECUTIVE 2.0 QUALITY COMMITMENT

"How to do"- Document ACTIVE PHARMACEUTICAL INGREDIENTS COMMITTEE

GMP Issues for Start-Ups, quality in the supply chain and role of the Qualified Person (QP)

SUPPLIER QUALITY MANAGEMENT SYSTEM QUESTIONNAIRE

Compliance Control Procedure Execution Management System Reduces Compliance Risks by 10X

On-Site GMP Training GMP COMPLIANCE TECHNICAL

FDA Inspection Observations The FDA 483 and Beyond. Objectives

Harmonizing Change Control Processes Globally

Standardizing Best Industry Practices

Title:: Effective GMP AUDITS for APIs and Formulation Pharma Companies By G.Sundar-Director/Consultant PharmQA Compliance solutions

Computerised Systems. Seeing the Wood from the Trees

EU GMP Requirements - Quality Systems - Bernd Boedecker GMP Inspectorate of Hannover / Germany at Turkish Ministry of Health Ankara, Oct 2009

Supplier Quality Assurance

Quality Management System Manual ISO9001:2008

JANUARY 2013 PREPARATION OF A SITE MASTER FILE FOR A MANUFACTURER OF COSMETIC PRODUCTS

Section 3-9: Principle 7: Record- Keeping Procedures

Quality Risk Management The Pharmaceutical Experience Ann O Mahony Quality Assurance Specialist Pfizer Biotech Grange Castle

Transcription:

Rx-360 Supplier Assessment Questionnaire (SAQ) The Rx-360 Supplier Assessment Questionnaire (SAQ) was created by the Rx-360 Supplier-Led Working Group. The Supplier-Led Working Group is an Rx-360 working group consisting of members from both pharmaceutical companies and leading suppliers to the pharmaceutical industry. Through this Working Group, members can share perspectives and work collaboratively to achieve greater harmonization and efficiencies in the supply chain to better serve patients. Pharmaceutical manufacturers and industry suppliers recognize the inefficiency and waste of resources when each individual pharmaceutical company creates its own supplier assessment questionnaire. Suppliers routinely exhaust valuable resources continuously completing slightly different forms of substantially similar questionnaires. In order to create the current SAQ, the Working Group analyzed numerous sample questionnaires submitted by Rx-360 members. In addition to standardized content, document formatting and question completion was optimized for accuracy and ease of completion by suppliers. The Rx-360 SAQ covers standard information that would be included in most supplier assessment questionnaires. The 4-part questionnaire is more detailed than most, but will decrease the number of times that questionnaires will need to be filled out by the supplier, while significantly decreasing the turn-around time back to manufacturers. The SAQ consists of four (4) modules: 1. General Company Information 2. Specific Site Information 3. Product Supplier Appendix 4. Services Supplier Appendix This document is module 2: Specific Site Information. Guidelines for Use Each company using the Rx-360 SAQ will still need to interpret, assess and score the questionnaire as they have done with their previous questionnaires. The Rx-360 SAQ is intended to make the collection of relevant information more consistent and efficient. Individual companies are still responsible for evaluating the questionnaires, determining any risk to their products, and following up with suppliers for more information as needed. Suggestions for Suppliers: A. Complete the module on General Company Information ahead of time and have it immediately available for manufacturers upon request. B. Complete this Specific Site module ahead of time for each manufacturing/packaging site within your company and have them immediately available for manufacturers upon request. C. Complete Product and/or Service Specific modules ahead of time for high-demand products so that they can be immediately available for manufacturers upon request.

NOTE: Upon request, the pre-completed Company module can be matched with the Site and Product/Service specific modules that the requesting manufacturer is requesting information on. This can make the qualification much more efficient and streamlined for all parties D. Lesser requested products can be completed upon request and matched with the precompleted Company and Site specific modules. E. Use the Rx-360 SAQ for requesting information from your own suppliers. F. Accept the Rx-360 SAQ from other suppliers and manufacturers. G. Keep the modules updated with the most accurate information on your company, sites, and products. H. Suppliers with highly specialized sites or products may also attach relevant appendix to supplement the information provided. I. Send comments, corrections, and suggestions for improvements to the Rx-360 SAQ to info@rx-360.org. Suggestions for Manufacturers: A. Alter procedures within your company as needed to send out the Rx-360 SAQ for requesting information from your own suppliers rather than a full customized questionnaire. B. Accept the Rx-360 SAQ from suppliers and manufacturers. C. The current Rx-360 SAQ is very comprehensive, but if you find there are highly specialized questions that are needed by your organization, consider creating a short appendix that can be sent along with the Rx-360 SAQ rather than not supporting the use of the standard SAQ. D. Send comments and suggestions for improvements to the Rx-360 SAQ to info@rx- 360.org. The Working Group believes the Rx-360 SAQ will create helpful efficiencies for both suppliers and pharmaceutical manufactures alike by: (i) (ii) (iii) Eliminating time-consuming redundancies Streamlining the process of approving suppliers Allowing comparative analysis of basic information. We strongly encourage Rx-360 supplier members to use the Rx-360 SAQ for their supply sites and Rx-360 pharmaceutical manufacturers to incorporate the Rx-360 SAQ into their supplier assessment process moving forward. Through this greater harmonization and efficiency in the supply chain we can all better serve patients. Kind regards, Rx-360 Supplier-Led Working Group Co-Chairs Rick Calabrese, Sartorius-Stedim rick.calabrese@sartorius-stedim.com Gary Perkins, Sigma Aldrich gary.perkins@sial.com 2

Rx-360 Supplier Assessment Questionnaire: Site-Specific Information SECTION 1. General Site Information 1.1 Site or Facility-Specific Name: 1.2 Address: GPS Coordinates: 1.3 Phone: 1.4 Email: 1.5 Fax: 1.6 Website: 1.7 If there is an individual contact for the following areas, please provide name and preferred contact information (at a minimum, name and telephone number or email): Quality: Technical Services: Commercial/Business/Sales: Primary Site Contact: 3

SECTION 2. General Site Operating Information 2.1 How many years has the site been in business? 2.2 What is the primary activity of the site? (e.g. manufacturing, distribution, etc) 2.3 To which, if any, subdivision of the parent company does the site belong? 2.4 Size of site (in sq. ft. or m.): 2.5 Please list or attach the normal hours/schedule of the facilities, including shutdown dates (if applicable): 2.6 Total number of employees on site: 2.7 Total number of employees in Quality Unit? 2.8 Total number of employees in Manufacturing: 2.9 What quality management system is utilized on site? ISO 9001 ISO 13485 21 CFR Part 210/211 21 CFR Part 820 European GMP, Eudralex Volume 4 Part I European GMP, Eudralex Volume 4 Part II ICH Q7 HACCP ISO 22000 Other or Home-Grown system Which Regulatory Initiatives does the site follow/comply with? REACH RoHs Ca Prop. 65 WEEE 2.10 Does the company have an export license? Yes No N/A 4

SECTION 2. General Site Operating Information 2.11 Is the site registered with any government regulatory agency (FDA registration, GMP certification, etc.)? If yes, please specify. 2.12 By whom is the site inspected (regulatory or third party) and list inspections within the last three years: 2.13 How often, as an annual average, is the site audited by customers or third parties? 2.14 Please list regulatory sanctions impacting the site within the last five years (i.e. warning letters, CEP suspension, import alerts, etc.): 2.15 Have there been any market withdrawals or consent decrees over the past two years? 2.16 If yes, please list and describe: Yes No N/A 2.17 Does the site outsource any quality-related activity? Yes No N/A 2.18 If answering yes to question 2.17, please specify the activities: 2.19 If answering yes to question 2.17, are any of the following subcontractor controls in place: 2.19a Quality Agreements with Suppliers Yes No N/A 2.19b Subcontractor Qualification/Audit Program Yes No N/A 2.19c Periodic Review of Supplier Performance Yes No N/A 2.19d Supplier Feedback Program 2.19e Raw Material Supplier List Yes No N/A Yes No N/A 5

SECTION 2. General Site Operating Information 2.20 Additional Comments: SECTION 3. Objectionable Materials on Site 3.1 Does the site or production plant produce, process or store any of the following: 3.1a Beta-Lactam Antibiotics 3.1b Pesticides 3.1c Cytotoxins 3.1d Steroids and/or hormones 3.1e Herbicides 3.1f High potency compounds 3.1g Materials of animal origin/biologics 3.1h Live virus or micro-organism 3.1i Allergens 3.1j Genetically Modified Organisms (GMO) 3.1k Agrochemicals 3.1l Other (Please specify): 3.2 If yes, are any of the following cross-contamination controls in place? 3.2a Dedicated Facilities 3.2b Access Controls 3.2c Dedicated Personnel 3.2d Dedicated Gowning 3.2e Procedural Controls 3.2f Other (please specify): 3.3 Additional Comments: SECTION 4. Site Operating Policies 4.1 Does the site utilize the following written policies, programs, or procedures? 4.1(1) Environmental, Health, and Safety 4.1(2) Facility Environmental Control Policy 4.1(3) Quality Control/Quality Management Policy 4.1(4) Quality Manual 6

SECTION 4. Site Operating Policies 4.1(5) Periodic Product Quality Review 4.1(6) Disaster Recovery Plan 4.1(7) Pandemic Preparedness Plan 4.1(8) Supply Chain Emergency Preparedness Plan 4.1(9) Business Continuity/Contingency Plan 4.1(10) Master Validation Plan 4.1(11) Risk Assessment Program 4.1(12) Supplier Approval Procedure 4.1(13) Monitoring and Review of Approved Suppliers 4.1(14) Mechanism to Reduce Testing 4.1(15) Receiving Incoming Inspection 4.1(16) Change Control Procedures 4.1(17) Document Management Policy 4.1(18) Document Retention Policy 4.1(19) Change Notification Procedures for Clients 4.1(20) General Facility Cleaning Procedures 4.1(21) Hygiene and Sterilization Procedures 4.1(22) Validated Equipment Cleaning Procedures 4.1(23) Preventative Maintenance Program/Procedures 4.1(24) Pest Control Program 4.1(25) Master Production Procedure 4.1(26) Control of Nonconforming Material 4.1(27) Deviation/Investigation Procedure 4.1(28) Out of Specification Policy and Procedure 4.1(29) Sampling Procedure/Sampling Plan 4.1(30) Raw Material Retention Program 4.1(31) CAPA Procedure 4.1(32) Label Control and Accountability 4.1(33) Product Release Procedure 4.1(34) Employee Training Program 4.1(35) Stability, Expiration, and Shelf-Life Program 4.1(36) Product Retention Program 4.1(37) Recall Procedure 4.1(38) Customer Complaint Handling 4.1(39) Equipment validation/qualification procedure 4.1(40) Internal audit/self-inspection program procedure 4.1(41) Site Security/Site Access Control Policies 4.1(42) New Hire Program/Induction Program 4.2 Additional Comments: 7

SECTION 5. Quality Assurance and Production 5.1 Does the site have an independent and defined Quality Assurance/Quality Management Division? 5.2 Does QA/QM have authority over the following: 5.2a Policies and procedures? 5.2b Review of documentation for release? 5.2c Release or rejection of incoming materials? 5.3 Does QA/QM investigate and resolve quality complaints? 5.4 Does QA/QM investigate and resolve internal deviations? 5.5 Does the QA/QM have the authority to assign a disposition to materials? 5.6 Does the QA/QM review manufacturing and testing records prior to release? 5.7 Does the facility utilize computerized systems for managing GxP activities or data? 5.8 Are relevant computerized systems 21 CFR part 11 and EU GMP annex 11 compliant? 5.9 Does the site use statistical methods for consistency and uniformity? 5.10 Does the site use controlled documents for following and recording manufacturing instructions? 5.11 Does the company qualify and/or validate manufacturing procedures? 5.12 Is any environmental monitoring conducted in production/finishing areas? 5.13 Does the company supply BSE/TSE declarations (if applicable)? 5.14 Does the company supply a declaration of Elemental Impurities (if applicable)? 5.15 Are ICH Q3C(R4) solvents used in the manufacturing process of supplied materials (if applicable)? 5.16 Are stability studies carried out according to ICH guidance? 5.17 Are solvents and mother liquor reused/recycled? 5.18 Does the site have a process water treatment system? 5.18a Please check all that apply to the system: City/potable water Distilled water Water for injection (WFI) Reverse Osmosis Clean steam Ultra-filtrated water (purified water) Other: Yes No Not Applicable 8

SECTION 5. Quality Assurance and Production 5.19 Does the site have a batch/lot system? 5.19a Is the system traceable? 5.19b Is it unique? 5.19c Is batch/lot manufacturing continuous? 5.19d Is manufacturing batch by batch? 5.20 Does the company perform on-site audits prior to approving critical GxP suppliers? 5.21 Does the company audit critical GxP suppliers after initial approval? 5.22 Does the company inspect incoming materials? 5.23 Does the company test incoming materials to defined specifications? 5.24 Does the company establish purchase specifications for raw materials? 5.25 Is the equipment multi-use? 5.26 Does the company qualify equipment installation? 5.27 Does the company qualify equipment operation? 5.28 Are production critical use instruments calibrated regularly? 5.29 Is rework or reprocessing allowed? 5.30 Are manufacturing and packaging activities fully traceable to the equipment, areas, and materials used? 5.31 Are production materials handled and stored in a manner to prevent degradation, contamination and cross-contamination? 5.32 If answering not applicable for any of the above, please elaborate: Yes No Not Applicable 5.33 Additional Comments: SECTION 6. Laboratory Procedures N/A for this Site 6.1 Does the site have standard procedures for handling, retaining and re-testing samples? 6.2 Does the site have written and approved specifications and test methods? 6.3 Are laboratory critical use instruments calibrated regularly? 6.4 Is there a standard procedure in place for analytical method generation? 6.5 Does the company qualify and/or validate analytical test procedures? 9

SECTION 6. Laboratory Procedures 6.6 Does the site perform stability testing on materials and/or products? 6.7 Are retention samples of key raw materials maintained? 6.8 Are standards traceable to their preparation and reagents used? 6.9 Are retention samples of finished product maintained? 6.10 Are shelf life/retest/expiration dates available and standardized? 6.11 Does the company provide a certificate of analysis (CoA) and/or a Certificate of Conformation/Compliance (CoC) for each lot or batch? 6.12 Does the CoA/CoC contain the manufacture name and location? 6.13 Does the CoA/CoC signed/e-signed by a Quality representative? 6.14 If a repacker performs analyses, will the Certificate reflect both the original manufacturing site data as well as the repacking site data? 6.15 If answering not applicable for any of the above, please elaborate: 6.16 Additional Comments: SECTION 7. Packaging, Storage, and Transport N/A for this Site 7.1 Does the site have a validated or qualified site labeling system? 7.2 Is the labeling system 100% verified? 7.3 Are batch production records retained and available? 7.4 Are packaging and labeling areas separate from production? 7.5 Are barcode readers in use and challenged regularly? 7.6 Are vision systems in use? 7.7 Is product ever packaged without a label being initially applied (i.e. bright stocking)? 7.8 Do labels include shelf life/expiration dates? 7.9 Do labels include lot/batch number? 10

SECTION 7. Packaging, Storage, and Transport 7.10 Do labels include requirements for storage conditions? 7.11 Is tamper evident seal used for each container of supplied materials? 7.12 Does the company use a First-In-First-Out or First-Expiration-First-Out system? 7.13 Does the company maintain and monitor specialized storage conditions? 7.14 Does the site make available a description of storage and/or warehouse conditions? 7.15 Does the company distribute products via a third party? 7.16 Are good distribution policies implemented? 7.17 Are transport mechanisms dedicated? 7.18 Does the company validate shipping method? 7.19 Does the company validate packaging methods? 7.20 If answering not applicable for any of the above, please elaborate: 7.21 Additional Comments: I (Supplier) confirm that the information provided in this questionnaire is correct and can be verified. Printed Name: Signature: Date: Title: Telephone Number: Email address: 11