Audit Training

VINCERT's Two Day's ISO 9001 Internal Quality Auditor WHO SHOULD ATTEND? This two (2) day course has been developed to provide delegates with the knowledge to begin performing internal quality audits. Case studies and participatory activities are based on the ISO 9001 quality system standard. At the end of the course delegates will be able to. Develop an internal audit system Perform internal audits to the requirements of ISO 9001 Understand how to get value for money by conducting internal audits Understand how to perform internal audits to ensure continuous improvement Quality Managers, Quality Engineers, Departmental Managers, and any other professional, technical or administrative personnel who have responsibility for managing an internal audit system or who are required to carry out internal quality audits in accordance with ISO 9000 quality management system requirements. Prospective course delegates should have some knowledge of the principles of Quality Assurance and the content and purpose of the ISO 9000 series of standards. WHAT YOU WILL LEARN By the end of the course you will be able to understand : Basic concepts and definitions ISO 9000 fundamentals Audit programming Responsibilities of an auditor Auditor selection and characteristics Performing an internal audit Reporting the audit Corrective action and follow-up COURSE CONTENT AND STRUCTURE Course starts at 9:30 A.M. and ends approximately at 6:00 P.M.. The course includes a series of presentations, Examples and Exercises involving group activities. Maximum attendance 20 Delegates. Eligibility? No specific knowledge or experience is required. COURSE Facilitators All course facilitators are highly qualified and experienced both in training and assessment of quality management systems. We strongly believe that the experience in Quality Management Assessment and Training skills is a right combination to deliver a practical training course. They are selected on their ability to make VINCERT courses both practical and enjoyable. How to Apply ? To apply for this course please obtain/download our Participant Nomination Form and mail to sameermodi@vincert.in or APPLY ONLINE. Please make advance payment* to reserve a seat in our course. For any cancellation please request at least 2 days in advance to the commencement of the course. Transfer of Nomination is acceptable.

VDA 6.3 Process Audit Training Service

It is necessary for a company to expertly carry out training audits. Risen Consultancy helps firms in conducting such training audits and suggests areas of non-compliance using principles of Quality Management System, fulfilling ISO /OSHAS norms.

Engaged in offering services such as security and audit related trainings .

Permit to Work (PTW) Audit and Training ensures high-risk operations such as hot work, confined space entry, electrical tasks, and working at heights are strictly authorized, risk-assessed, and safely executed.

We can help you make your training and development processes more effective by professionally analyzing each and every document, improving it, and adding more value to it. Apart from the documents, we will also analyze how your training programs are conducted and give you viable suggestions on how to generate more value out of each training program, so that your employees grow along with your firm.

S. Panse & Co. is a speciality firm of Chartered Accountants in India, focused on Financial Sector, particularly, Banks,Mutual Funds, Insurance, Portfolio Management Services and Other Intermediaries in the Capital Market of India.

Competence enhancement is the nead of the day. Agile Group has a team of Professionals with over 100 years of Cumulative Experience. These expereinced professionals have decided to pay back the Industry and society the knowledge and learning they have gained in form of Structured Training programs on various topics including Management System Standards like ISO 9001; ISO 14001; OHSAS 18001; ISO 20000: ISO 22000: ISO 27001 to name a few. In addition, Agile Group also provides soft skills training on various topics inclidng Personal Effectiveness; Transactional Analysis; Analytical Skills; Team Management Skills, etc..

Audits: Raaj GPRAC provides a multitude of training services through audits as well. The audit exercises include compliance assessment and advisory activities at clients offices and premises. Our audits include the following: A. Regulatory Compliance Audits and ISO Certification: We assist clients to prepare for an imminent regulatory inspection by carrying out one or more mock regulatory audits in advance of the real thing. Our consultants visit the facility and carry out an inspection in the style of the relevant regulatory body (Local (Indian) FDA, US-FDA, MHRA, EMEA etc.) after which we will provide An in-depth, impartial and professional assessment of their current state of compliance.A detailed, prioritized action plan for the rectification of areas of non-compliance and vulnerability.Staff coaching in the sorts of questions which are likely to be asked during the inspection and how best to answer them.GMP Gap analysis auditWe visit the client site and perform an audit to determine where one needs to improve processes, documentation, and operations. We have experienced people able to perform GMP Audit Readiness/GMP GAP assessments for the clients facility against GMP requirements. We also offer assistance in correcting any deficiencies found. B. Good Clinical Practice (GCP) Audits 1. Adequacy of Systems / System AuditsA bird s eye view of the system to assess major process gaps and select the key systems impacted in the fields of Clinical Research, Quality Assurance and Pharmacovigilance for Phase I to IV studies.Looking into the adequacy of the Standard Operating Procedures with respect to regulatory requirements and suggestion for new SOPs.Vendor management SOPs and frequent quality checks of the vendors.2. Investigator site and sponsor/CRO file auditsAudit Plan development based on risk assessment of the study and the site performanceConduct a detailed review of all essential documents related to study conduct for the selected sites for audit preparationConduct Investigator site auditPrepare and send audit reports (one per site) to clinical research team.Training We provide in-depth training and workshops on the courses and programs that are at par with the current trends of the pharmaceutical industry. Our courses and programs are designed to leverage your career options and hone your expertise in the various aspects related to the pharmaceutical industry. We conduct Training and Workshops on RA/ QA/ AD/ FD/ ICH/ CTD/ eCTD/ ACTD/ 21CFR parts/ GMP/ GLP/ GCP, with Case Studies, Exercises, Questionnaires. The following are the major highlights of our workshops and training programs:Dedicated and comprehensive guidance and counseling of Pharmacy studentsTraining and Development of Pharmacists, RA, QA, Clinical AssociatesGrooming and mentoring future leaders in Pharmaceutical industry s various aspects like RA, QA and R DComplete support in successful audit preparation for WHO-GMP, USFDA, UK-MHRA and the like.Technical Support in helping students understand the logistics and ground realities of DCGI FDA activitiesSupport in Clinical SubmissionsGMP CGMP training to workmen, operators, and supervisory staffFDA GMP centric training courses materialsGMP Training Program modules on topics such as Good Documentation Practices, cGMP Basics and cGMP Advance that you can use for your ongoing training needs.Onsite or Classroom training to Pharmaceutical, Biotech industries, and Food industries to Officers, Executives, Managerial staff from Production, Warehousing, QA, QC and Marketing followed by evaluation.

Optimum F&SReduced LiabilityReduced ManpowerTimely Completion of Projects

Well experienced. Result oriented. Proven and effective trainings. Highly Motivated ** Zeal ** Passion ** DedicatedLive Wire Workshop. Lisam Training, your satisfaction.Small - Medium - Large enterprise. Set your house in order through Lisam hawkeye audits.We are the first, to introduce AMC for safety audit.

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