Maribor‚ Slovenia SOP 6 CALIBRATION OF VERNIER CALLIPER GAUGES Issue date 11.7.2003 Issue No. E-1 Approved by Bojan Ačko‚ Ph.D. Changes made AMENDMENT REMOVED No. Section Date ADDED Page Issue No. Section Present issue E-1 is equal to the issue No. 3 dated September 1998 Page Issue No. CONTENTS 1 1.1 INTRODUCTION General aspects 4 4 2 MEASURING EQUIPMENT 4 3 RECEIPT 4 4 CLEANING 4 5 THERMAL STABILISATION
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CASE STUDY ON TECHNOLOGY PLANNING AND IMPLEMENTATION 1. Introduction Airport operations are growing in complexity day by day‚ and extend across multiple service providers at the airport – namely ground handlers‚ customs‚ immigration‚ retail tenants‚ air traffic control‚ security‚ baggage handlers‚ airlines consortiums and airlines. These agencies use the airport infrastructure in such a way that they meet their commitment to their customers in due time. These commitments put a lot
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Accommodation Management Staffing The housekeeping department of a hotel is responsible for ‘cleanliness‚ maintenance‚ aesthetic upkeep of rooms‚ public areas‚ back areas and surroundings.’ The department is not always given the respect it is due in terms of work load‚ the size of which can be estimated by the fact the department often employs the largest workforce. There are a variety of areas the housekeeping department must manage‚ the following table taken from Hotel Housekeeping Operations and
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SIX MONTHS INDUSTRIAL TRAINING TRAINING REPORT UNDERTAKEN AT NEW HOLLAND FIAT INDIA PRIVATE LIMITED IN TRACTOR ASSEMBLY ON AVERAGE DEFECT PER UNIT CONTROL SUBMITTED IN PARTIAL FULFILLMENT OF THE DEGREE OF BACHELOR OF TECHNOLOGY IN MECHANICAL ENGINEERING Under the Guidance of: Submitted By: Name: Mr. Rahul Gupta Name: Danveer Sharma Designation: Manager College Roll No.: 90351126186 Department: Tractor
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Appendix A: HACCP PLAN Company name: Kegworth’s stuffed turkey roll Purpose Statement: This manual detail the stuffed turkey roll manufactured in this establishment and provides a full description of the hazards‚ preventative measures‚ corrective actions‚ and verifications used in the safe manufacture of the product at this establishment. Commitment Statement: The owners of this establishment by signature agree to accept and perform the duties described in the HACCP manual and further
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ROHAN TRIVEDI FINAL YEAR B.PHARM ROLL NO: 60 CONTENTS 1 | INTRODUCTION | 2 | COMPANY ORGANISATION | 3 | COMPANY PREMISES | 4 | DOCUMENTATION | 5 | RAW MATERIAL AREA | 6 | PRODUCTION * AMPOULE FILLING * VIAL FILLING * DRY POWDER FILLING | 7 | QUALITY CONTROL | 8 | CONCLUSION | A Brief Introduction To Industrial Training Industrial training is nothing but a certain period of practical training in a drug manufacturing industry. Industrial training is purposely asked
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A Seminar on Validation Of Sterilizing filter‚ Capsule filling machine & Integrated Lines Prepared By Guided By: DAVE JAY Mr.RajeshParmar sir M. Pharm QA‚ Sem – III APMC COLLEGE OF PHARMACEUTICAL EDUCATION AND RESEARCH. (QA Department) Equipment qualification Equipment qualification / validation includes following things User
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INTRODUCTION Hotel industry is one of the primary and leading industry in the service sector nowadays Because it caters directly to all the needs and satisfactory of a guest or customer . As what I had said this is a primary and leading industry in our generation today‚ so we expect a lots of competitors‚ and that’s the big reason why we should keep our establishment unique from other. Unique is a key word that we need to get
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(FRAGORD) to conduct an area reconnaissance. The OPORD specifies the focus‚ tempo‚ and engagement criteria for reconnaissance. Communications have been established and information is being passed in accordance with (IAW) the standard operating procedures (SOP). The unit is provided guidance by the rules of engagement (ROE). It may also have Mission Instructions‚ such as a peace mandate‚ Terms of Reference‚ and Status of Forces Agreement (SOFA). Coalition forces‚ noncombatants‚ government agencies‚ nongovernment
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Process validation Protocol and Report Chapter-1: Introduction In today’s highly regulated environment for development and manufacturing of Pharmaceutical /biopharmaceutical Drugs and medical devices there is a heavy requirement imposed by the regulatory bodies‚ for the manufactures of drug products to provide an appropriate amount of assurance that critical processes employed in producing a drug substance or drug product can be shown to be both doing the right job‚ and doing the job right is often
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