Understanding Governance, Risk, and Compliance Framework in Business
Governance, Risk, and Compliance (GRC) are essential components of a robust business strategy. Governance focuses on aligning objectives with stakeholder expectations, Risk Management involves identifying and mitigating threats, and Compliance ensures adherence to regulations. By integrating GRC pri
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Mandatory Vendor Compliance Training & Regulatory Requirements Overview
Welcome to ECMCC's mandatory compliance training for vendors covering regulatory requirements, compliance program overview, fraud Prevention, OMIG compliance, Code of Ethical Conduct, and communication policies. Learn about Stark Law, Anti-Kickback Statute, and False Claims Act for ethical conduct a
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Understanding CONFIA: The Brazilian Cooperative Compliance Program
Cooperative Compliance is a relationship between taxpayers and Tax Administration based on principles like good faith, collaboration, and transparency. CONFIA aims to provide legal certainty, prevent disputes, reduce compliance costs, and improve tax compliance through voluntary and cooperative deve
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The Crucial Role of Compliance in Payroll Management Software!
Payroll management software is essential for businesses of all sizes, automating processes like wage calculation and tax deduction. Compliance ensures adherence to legal frameworks, safeguarding against penalties and fostering trust. Key features include robust security measures, tax compliance capa
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India's Best Pharma Products Manufacturers in Chandigarh
Unimarck Pharma India's Best Pharma Products Manufacturers in Chandigarh. We are WHO-GMP, GLP, and ISO certified. 40 years of experience in this industry.
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CPGP Study Guide and How to Crack Exam on Pharmaceutical GMP Professional
Click Here--- \/\/bit.ly\/4bsglWA ---Get complete detail on CPGP exam guide to crack Pharmaceutical GMP Professional. You can collect all information on CPGP tutorial, practice test, books, study material, exam questions, and syllabus. Firm your knowledge on Pharmaceutical GMP Professional and get r
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Pharma Franchise For All Pharma Products All Over India
Unibiotech Formulations offer different types of Pharma products all over India for PCD Pharma Franchise. Unibiotech is WHO-GMP certified Pharma Franchise company. Call us Today @ 917814301804, 919216901651.\n\n\n
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ASQ Pharmaceutical GMP Professional (CPGP) Exam | Boost Your Score
Click Here---> \/\/bit.ly\/4bsglWA <---Get complete detail on CPGP exam guide to crack Pharmaceutical GMP Professional. You can collect all information on CPGP tutorial, practice test, books, study material, exam questions, and syllabus. Firm your knowledge on Pharmaceutical GMP Professional and get
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Pharmaceutical Manufacturing Company in India | Unimarck
Our focus is to provide reliable manufactured products that are well-certified by reputable organizations like WHO and GMP. To provide a diverse range of products like quality tablets, syrups, and capsules, our company is working hard to meet high standards in its manufacturing process.
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Top PCD Pharma Franchise Company in India | WHO GMP Certified
Unibiotech Formulations is WHO GMP Certified Pharma Franchise Company in India. We offer Latest formulations in tablets, capsules, suspensions, syrup, etc. Get more info for franchise Services Contact us at 917814301804
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RRH Student Re-Entry Process for Clinical Requests & Compliance
The RRH Student Re-Entry Process outlines steps for clinical request processing, approval, and compliance requirements for various disciplines within the nursing program and other departments. It includes sending requests to the Nursing Institute, communication procedures, compliance documentation,
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Understanding GMP Audits in Construction: Navigating Client Expectations
This presentation at the National Association of Construction Auditors' virtual conference focuses on helping clients grasp the key objectives and processes of Guaranteed Maximum Price (GMP) audits. Dave Potak, a seasoned professional, will share insights on managing client expectations, best practi
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Guidelines for Personnel Training and Hygiene in Pharmaceutical Manufacturing
Personnel responsibilities in a manufacturing unit include training, hygiene, and maintaining personal records. Guidelines as per Sch.M of D&C act 1945 outline the supervision, qualifications, and duties required for technical staff, QC lab, and QA personnel. Health, clothing, and sanitation protoco
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Microbiological Quality Control in Pharmaceutical Environment
Microbiological products in pharmaceutical settings are influenced by the quality of materials and the environment. Good Manufacturing Practices (GMP) are essential to minimize contamination risks, with control points focused on the ecology of microorganisms. Sources of contamination include the atm
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Top WHO-GMP-ISO Certified Monopoly Pharma Franchise Company
Top WHO-GMP-ISO Certified Monopoly Pharma Franchise Company in India. Contact Unibiotech Formulations At 917814301804, 919216901651
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ASEAN Guidelines on GMP for Traditional Medicines: Evaluation of Corrective Action and Preventive Action
The ASEAN Guidelines on GMP for Traditional Medicines discuss the importance of Corrective Action and Preventive Action (CAPA) for maintaining quality in health supplements. CAPA involves identifying nonconformities, implementing solutions, and preventing future occurrences through continuous improv
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Enhancing Compliance Monitoring in South African Public Service
The Compliance Monitoring Framework developed by the Office of Standards and Compliance aims to improve adherence to public administration norms and standards in South Africa. This framework is designed to reduce non-compliance through ongoing supervision, investigation, and promotion of proper beha
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Effective Corporate Compliance Program Overview
Corporate compliance is essential to prevent fraud, waste, and abuse within organizations. This program aims to detect and prevent deceptive practices, unnecessary costs, and improper behaviors. Key elements include appointing a Compliance Officer, establishing policies and procedures, providing edu
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Managing Microbiological Quality in Pharmaceutical Environments
The quality of microbiological products is influenced by the pharmaceutical environment materials. Good Manufacturing Practices (GMP) play a crucial role in minimizing contamination risks. Various sources of contamination include the atmosphere, water, persons, raw materials, packaging, buildings, a
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Post Award Fiscal Compliance: Who We Are and What We Do
Post Award Fiscal Compliance (PAFC) assists campus and central administrative units in mitigating non-compliance risks with sponsor terms and conditions by monitoring compliance, interpreting award requirements, providing training, and enhancing internal controls. The team includes Matt Gardner, Ass
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WHO-GMP, GLP, ISO Certified Pharma Manufacturing Company
Unimarck Pharma is WHO-GMP, GLP, ISO Certified Pharma Manufacturing Company Since 1984. Contact us today at 91-172-2244500.
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Understanding Good Laboratory Practices (GLP) in Pharmaceuticals
Good Laboratory Practices (GLP) is a quality system ensuring non-clinical health and environmental safety studies are conducted accurately and reliably. GLP promotes the validity of test data for determining safety of chemicals, pharmaceuticals, food, and cosmetics. This article explores the definit
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ASEAN Guidelines on GMP for Traditional Medicines/Health Supplements - Preparation for Inspection
This content provides guidelines on preparing for a Good Manufacturing Practice (GMP) inspection for traditional medicines and health supplements in ASEAN countries. It covers activities such as planning inspections, forming inspection teams, reviewing documentation, preparing inspection plans, hold
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Glycomacropeptide Extraction and Casein Curd Formation from Skim Milk
This detailed study explores the extraction of glycomacropeptide (GMP) and securing casein curd from skim milk. It covers the composition of milk, the classification of milk proteins, the role of rennet in curd formation, and the history and preparation of rennet. Additionally, it delves into the us
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ASEAN Guidelines on GMP for Traditional Medicines - Preparation of GMP Report
The ASEAN Guidelines on GMP for Traditional Medicines provide detailed instructions on preparing GMP reports, including post-inspection activities, deficiency classification, examples of deficiencies, and inspection report format. Deficiencies are categorized as Critical, Major, or Minor, with speci
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ASEAN Guidelines on GMP for Traditional Medicines - Philosophy of Inspection
The ASEAN Guidelines on GMP for Traditional Medicines highlight the Philosophy of Inspection for ensuring quality and safety in traditional medicines and health supplements. The document covers legal terms, audit trail requirements, electronic signature control, and familiar auditor requirements. It
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Enhancing Feed Safety Through GMP+ International Certification
Explore the world of GMP+ International certification for feed safety, providing value to former foodstuffs. Learn how food companies can ensure safe feed practices, with a focus on compliance, incident management, and traceability. Discover the chain approach in various industries, from cultivation
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Importance of Compliance Training in Ensuring Ethical Business Practices
Compliance training at West Cancer Center plays a vital role in educating employees on laws, regulations, and company policies to ensure ethical conduct. With a commitment to compliance, the center's Code of Ethics emphasizes activities that adhere to laws and regulations, prioritize quality care, a
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Analysis of Boiling Target Study at Kent State University
Boiling Target Study conducted at Kent State University focused on analyzing the impact of beam current on target density fluctuations, termed as Boiling. The study involved applying various cuts, calculating live time, and extracting charge yield data to determine the presence of target boiling. Su
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ASEAN Guidelines on GMP for Traditional Medicines/Health Supplements: Conducting GMP Inspection
The ASEAN Guidelines provide detailed procedures for conducting GMP inspections to ensure objectivity and appropriateness. The inspection processes include opening meetings, facility inspections, documentation review, inspector meetings, and exit meetings. During the opening meeting, the inspection
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Pharma Franchise Company For Start Your Pharma Business
Pharma Franchise Company For Start Your Pharma Business. Unibiotech Formulations, a WHO-GMP certified PCD Pharma company in India. Call 7814301804, 9216901651 For Full Details.
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ASEAN Guidelines on GMP for Traditional Medicines - Classification of GMP Non-Conformance
Classification of GMP non-conformance is crucial for conducting inspections and preparing reports. It helps companies take necessary actions and affects the inspection rating. The guidelines outline critical, major, minor, and other deficiencies in traditional medicines and health supplements, empha
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Compliance and Sustainability Leadership Team Overview
This document provides an overview of the Compliance and Sustainability Leadership Team structure, including key positions such as Global Director, Head of Compliance and Sustainability Standards, and various advisors and managers responsible for safety, health, compliance, ethics, and risk manageme
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Compliance Assurance Report on Dental Services in Q1 2024
A compliance assurance report was conducted on dental services in Q1 2024 as part of the HSE Children First Compliance Assurance Checks. The report highlighted areas of compliance and partial compliance, with efforts noted to meet Children First requirements. Areas of improvement were identified in
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Importance of Personnel Hygiene in Dairy Plant Management
In a dairy plant, maintaining good manufacturing practices (GMP) is crucial for ensuring quality and safety of products. This includes emphasizing personnel hygiene, cleanliness, and preventing contamination. Employees must adhere to strict personal hygiene practices, such as proper grooming and wea
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Interim Waiver Process for BRC Audits During Corona Outbreak
This content outlines the interim waiver process and scheduling procedures for local office client audits during the Corona outbreak. It includes steps for completing waiver applications, conducting remote audits, and handling certification extensions. The document also provides guidelines for remot
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RAC Exam I Test Questions
The RAC Exam I Test Questions cover various aspects of regulatory affairs and compliance in the pharmaceutical industry. The questions touch on topics such as GMP, FDA regulations, product approvals, and legal requirements. Test your knowledge with these 100 questions to enhance your understanding o
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ASEAN Guidelines on GMP for Traditional Medicines - Preparation for Inspection
This content outlines the preparation activities for a Good Manufacturing Practice (GMP) inspection for Traditional Medicines/Health Supplements as specified by the ASEAN Guidelines. It covers the objectives, processes, inspection team formation, documentation review, and other key aspects involved
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Compliance Testing by ERA for IT Systems Developed and Deployed for TAF TSI
Compliance testing for IT systems developed and deployed for TAF TSI involves checking if messages comply with TAF XSD and basic parameters, assessing compliance of IT tools against TSI requirements, and issuing compliance assessment reports. The process includes testing messages for mandatory eleme
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Addressing Compliance Challenges in Ottawa's Housing Sector
Ottawa's housing organizations face compliance challenges related to fire safety, including lack of code adherence, non-compliance issues, and legacy structural issues. Efforts to achieve compliance involve daily inspections, addressing combustible materials and obstructions, and obtaining funds for
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