Francis Lamm
Francis Lamm holds an A.A.S. in Electronic Engineering Technology from the Central Technical Institute of Electronics and the American Society for Quality has certified him as a Quality Manager. Mr. Lamm brings over forty-five years of experience to the KAVON team. In that time, he has achieved countless benefits for his clients, including material review and scrap reduction programs for clients. This efficiency has helped them save over $250,000. Furthermore, he has lead countless clients to ISO 9001:2000 and ISO 13485 certification. He brings the expertise FDA current good manufacturing programs (CGMP) and Quality System Regulations, among many other things, to the KAVON team.
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Meetings
Meeting Guidelines
By Francis Lamm
Formal and informal meetings are a necessary part of the workday for organizations of all sizes and in all sectors of businesses providing a myriad of products and services. They are useful to discuss and resolve important issues and to convey information to all concerned parties at the same time, particularly when instant feedback is essential. While productive meetings have their place, from time to time, too many of us have been involved in long drawn-out meetings that stray off subject or accomplish little or nothing except waste time that could be better spent doing our primary job responsibilities. Other times, non-productive meetings occur when attendees are not sufficiently prepared, haven’t done required research, made up handouts when required, or when some individuals tend to monopolize meetings with non-essential subjects.
For maximum effectiveness and productivity, the following are general guidelines for conducting formal meetings that meet the requirements for FDA/GMP, FAA, Military, Governmental Agency, ISO/TS/AS requirements and Good Business Practices.
GENERAL FORMAL MEETING GUIDELINES:
- Depending on the topic and preparation needed, initiators send out a meeting notice 3 to 10 working days in advance with a proposed agenda of discussion, action items, inputs, reports due, and required attendees.
- Start and end meetings on time.
- Assign someone to take and record meeting minutes/summaries.
- Take and record attendance.
- Everyone is to be prepared to discuss the agenda items, summary reports, handouts, new discussion items, etc.
- Avoid detailed reports. All status reports are to be brief summaries. If detailed reports are necessary, call a separate meeting of interested parties to discuss report details.
- Advise the receptionist and front office with names of attendees.
- Minimize meeting interruptions (sign-offs, phone calls, non-emergencies, etc.)
- Set a projected meeting time limit and end on time.
- Follow the meeting agenda and stick to it.
- Minimize or defer side discussions of limited group interest. Set time limits for presentations and discussions.
- Observe common business courtesies at all times.
- Record minutes of meeting in sufficient detail, including action item assignments and follow-up activities, deadlines, corrective actions, new items, etc.
- Set advance date(s) for next scheduled and side discussion meetings, as applicable.
- Distribute meeting minutes to participants and copy interested parties within five working days.
- Maintain record files of meetings for history files, as reminders of required activities and as documented evidence of what took place, when, why, where, who attended, and assigned follow-up action assignments.
NOTE: If formal and informal business & production meetings are not adequately documented in writing and distributed for historical purposes, there is no evidence the meetings ever took place for regulatory purposes. Individuals’ hand-written notes that are not distributed do not suffice.
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KAVON International, Inc. is a business consultancy that helps clients create Value in order to attain and sustain a Competitive Advantage in the markets they serve. If your company is seeking registration or compliance to any of the Quality Management System standards such as ISO 9001, ISO/TS 16949, AS9100, ISO 17025, ISO 14001, or ISO 13485, or wants to establish a continual improvement program using Lean Six Sigma methodologies, give us a call and let one of our Trusted Advisors help you with implementation and training.
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