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  • RETSCHLaboratory Mills Crushers and Sieve Shakers

    Laboratory Mills Crushers and Sieve Shakers. RETSCH is the leading solution provider for neutral-to-analysis sample preparation and characterization of solids. Based on a century of experience RETSCH develops size reduction and sieving equipment which is characterized by excellent performance operating convenience safety and a long lifetime.

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  • Laboratory Quality Management System Handbook

     · laboratory assessment laboratory customer service occurrence management process improvement quality essentials laboratory process control clinical laboratory ISO 15189. Key words. Note Health laboratories in this handbook is a term that is meant to be inclusive

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  • Materials Basic CGMP RequirementsFDA

     · Quality Production Laboratory Materials Facilities and Equipment Packaging and Labeling § 211.80General Requirements (a) There shall be written procedures describing in

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  • NASANASA Glenn Research CenterPlum Brook Station

     · A unique wind tunnel designed to test air-breathing propulsion systems at speeds exceeding 5 times the speed of sound. Before Orion carries the next generation of explorers into space it must withstand rigorous tests in the world s largest vacuum chamber. NASA tests solar sails the propulsion system of the future at Plum Brook Station.

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  • Design Qualification FDA MHRA WHO cGMP EU FLCV

    Design Qualification Rationale. A Design Qualification protocol is used at the stage where a design that has been developed from the VMP / URS /GAMP 5 / cGMP / and other Health and Safety Guidelines is reviewed and documented by competent persons to ensure that the designed equipment if built will satisfy all the detailed specified requirements as contained in the VP and URS.

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  • Health Department Forms

     · Laboratory Personnel Qualification Appraisal. pdf 18k. doc 103k. OCC-34. Clinical Laboratory Report of Elevated Levels of Heavy Metals Lead In Adults (Greater than 16 Years of Age)Arsenic Cadmium Mercury In Persons of Any Age. pdf 15k. doc 48k. Blood Bank Licensure and Regulatory Compliance. Form #.

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  • Facilities and Equipment CGMP Requirements

     · Objectives • Facilities and Equipment CGMP Highlights • Aseptic Manufacturing Facility • Equipment Qualification • Cleaning Validation . Quality Production Laboratory Materials Facilities

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  • Design Qualification (DQ) of Equipment Pharmaceutical

     · Design qualification is defined as a verification process on the design to meet particular requirements relating to the quality of pharmaceuticals and manufacturing practices. However the procedure for design qualification in pharmaceuticals is one reason as to why some products do not make it to the shelves in drugstores.

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  • Good Laboratory Practices (GLP) guidelines regulations

     · Good Laboratory Practices ( GLP) guidelines for MANAGEMENT PROCESS. 1. Personnel Sufficient number of qualified employees must be a part of this (Qualification can be relevant educational background experience or training). Apart from this job profiles tasks

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  • 18 LABORATORY QUALITY CONTROLEPA

     · 18 LABORATORY QUALITY CONTROL 18.1 Introduction This chapter addresses internal laboratory quality control (QC) the purpose of which is to monitor performance identify problems and initiate corrective action. If project requirements are more stringent than typical laboratory QC criteria the project manager and the laboratory should

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  • RULES OF ALABAMA STATE BOARD OF HEALTH

     · (g) "Director" means any qualified person responsible for administration of technical and scientific operations of a laboratory including supervision of testing procedures and result reporting. (h) "Independent Clinical Laboratory" means any laboratory which operates primarily independent of other

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  • Quality Control Manager Salary Duties and Requirements

     · Salary Information for Quality Control Managers. According to the U.S. Bureau of Labor Statistics (BLS) industrial production managers which is

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  • Lab Manager Job Description Duties and Requirements

     · Students who searched for Lab Manager Job Description Duties and Requirements found the following resources articles links and information helpful.

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  • Section 2Laboratory Equipment and Functions

     · Section 2 Laboratory Equipment and Functions 2 of 5 Iron ring Supports a beaker over a bunsen burner. Wire gauze is usually placed on top of this structure. Utility clamp Used to hold a test tube or other piece of equipment in place on a ring stand.

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  • Lab Technician Resume Sample (with Skills Job

     · Lab Technician Resume Sample (with Skills Job Description) Lab Technician Resume Sample (with Skills Job Description) You turn raw samples into science that helps people live longer. Show the hiring manager you re a centrifuge in a white coat with this standout sample lab technician

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  • Laboratory Manager Job Description Monster

    Laboratory Manager Skills and Qualifications Managing Processes Presenting Technical Information Management Proficiency Equipment Maintenance Training Analyzing Information Informing Others Quality Focus Clinical Lab Testing Lab Environment Technical Understanding

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  • LabOps Lab QualificationIdaho Transportation

     · Manager and request inspection and qualification for those test methods needed to perform the mix design. If a laboratory is located in another state qualification under the

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  • Installation Qualification/Operational Qualification

     · qualification should also be performed when the Experion electrophoresis station is moved to a new location when the software is upgraded and when the computer that runs the electrophoresis station is changed or modified. Operational qualification should also be run on a

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  • Clinical Laboratory Program Mass.gov

     · The Clinical Laboratory Program oversees the state licensure of clinical laboratories in Massachusetts and works as the State Agency that administers the Clinical Laboratory Improvement Amendment (CLIA) program on behalf of the Centers for Medicare and Medicaid Services (CMS) for the federal certification of laboratories.

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  • Classification Qualifications

    Classification Qualifications. Welcome to the U.S. Office of Personnel Management s Federal Position Classification and Qualifications website. This website provides Federal position classification job grading and qualifications information that is used to determine the pay plan series title grade and qualification requirements for most

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  • Point-of-Care Testing Guideline

     · manager educational coordinators laboratory managers quality assurance managers pharmacy managers and others who are needed to train end users implement the testing. A specific Point-of-Care Supervisor/Coordinator is recommended for larger institutions to monitor test results. Purchasing and information technology representatives should

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  • Production and Process Controls

     · Quality Production Laboratory Materials Facilities and Equipment Packaging and Labeling §21 CFR 211.110Sampling testing of in-process materials drug productsKey points

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  • STATE OF NEW JERSEY

     · 10 qualifications hereinafter set forth in federal regulations at 42 11 C.F.R. Part 493 subpart M may apply for examination for a 12 plenary license as a bio-analytical laboratory director. The 13 following qualifications as to education and experience are 14 established as prerequisites for application for examination or

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  • Qualifications to Serve on a Board of Directors Work

     · Serving on a board of directors is a major commitment that should not be undertaken lightly. In fact bank board director Charles J. Thayer writing in Directors Boards suggests that the potential risks of serving on a community bank board of directors can outweigh the rewards. Bank board of directors qualifications include understanding of banking laws because directors are expected to know

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  • Program Director job description template Workable

    Program Director responsibilities include Initiating and setting goals for programs according to the strategic objectives of the organization. Planning the programs from start to completion involving deadlines milestones and processes. Developing or approving budgets and operations.

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  • Laboratory Quality Management System Handbook

    laboratory assessment laboratory customer service occurrence management process improvement quality essentials laboratory process control clinical laboratory ISO 15189. Key words Note Health laboratories in this handbook is a term that is meant to be inclusive

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  • Design Qualification (DQ) of Equipment Pharmaceutical

     · Design qualification is defined as a verification process on the design to meet particular requirements relating to the quality of pharmaceuticals and manufacturing practices. However the procedure for design qualification in pharmaceuticals is one reason as to why some products do not make it to the shelves in drugstores.

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  • Defining Calibration Qualification of Equipment

    Operation Qualification (OQ) concerns itself with checking every function of the equipment to ensure that they are not deviating from the manufacturer s specifications. The process calls for extensive use of certified traceable simulators and standards for verifying

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  • SOFTWARE QUALIFICATION PROTOCOLAgilent

     · Design Qualification (DQ) Design Qualification (DQ) for commercial lab instruments is recommended by some but not all guidances and procedures. Defintions of DQ found in guidances and firm-specific validation procedures vary widely around the world. Some firms require

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  • Laboratory contamination Preventing contamination

     · Part two presented by Mary Kay Bates global cell culture specialist and Douglas Wernerspach business director Thermo Fisher Scientific is entitled Tips for preventing contamination. In the first part of this series we discussed types of biological contaminants and learned that laboratory personnel and procedural errors can be the greatest contamination sources but what can we do about it

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  • Agilent 1100/1200 HPLC ChemStation Operation

     · Lab Exercise Introduction to the HPLC ChemStation In this Laboratory You Will 2 In this Laboratory You Will • Access the HPLC ChemStation software and understand the purpose of each View. • Use the ChemStation Configuration Editor. • Learn about the Scheduler. • Learn how to maintain the HPLC ChemStation computer.

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  • Enclosed is the clinical laboratory licensure packet you

     · Definitions. laboratory director owner or other controlling authority for cited deficiencies and how the plan will maintain correction. .03(p) approval by the Department. The plan shall identify the existing noncompliance of the laboratory and the proposed Failure to follow

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  • STATE OF NEW JERSEY

     · 10 qualifications hereinafter set forth in federal regulations at 42 11 C.F.R. Part 493 subpart M may apply for examination for a 12 plenary license as a bio-analytical laboratory director. The 13 following qualifications as to education and experience are 14 established as prerequisites for

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  • GUIDELINES ON VALIDATION APPENDIX 6 VALIDATION

    Working document QAS/16.673 page 5 140 GUIDELINES ON VALIDATIONAPPENDIX 6 141 VALIDATION ON QUALIFICATION OF SYSTEMS UTILITIES AND 142 EQUIPMENT 143 1.144 Principle 2.145 Scope 3.146 Glossary 147 4. General 148 5. User requirement specifications 149 6. Factory acceptance test and site acceptance test

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  • Guidance for General Laboratory Safety Practices during

     · General Guidance. This guidance is to address the general workflow safety concerns of laboratory personnel during the COVID-19 pandemic. All laboratories should perform site- and activity-specific risk assessments to determine the most appropriate safety measures to implement for particular circumstances. In addition facilities should adhere

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  • Laboratory Manager Job Description Salary

    Laboratory Manager. Laboratory Manager plans and implements the overall laboratory policies procedures and manages services for a unit and/or shift. Ensures efficient and effective departmental operations including department quality control and compliance adherence. Being a Laboratory Manager may require a bachelor s degree.

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  • Defining Calibration Qualification of Equipment

    Operation Qualification (OQ) concerns itself with checking every function of the equipment to ensure that they are not deviating from the manufacturer s specifications. The process calls for extensive use of certified traceable simulators and standards for verifying the reliable and accurate processing of input parameters.

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  • EQUIPMENT QUALIFICATION PLAN (EQP)

     · SOP #123 Qualification of GCMS Systems. In Enterprise Edition the EQP has the same role as the traditional Qualification SOP. ii The traditional SOP provides lists of tests limits for the range of system configurations found in the lab or department. The EQP follows this concept.

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  • Laboratory contamination Preventing contamination

     · Part two presented by Mary Kay Bates global cell culture specialist and Douglas Wernerspach business director Thermo Fisher Scientific is entitled Tips for preventing contamination. In the first part of this series we discussed types of biological contaminants and learned that laboratory personnel and procedural errors can be the greatest contamination sources but what can we do

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  • RI Department of Health

     · If the director is not full time the name and qualifications of th edirector s designee must be also submitted. 3. Laboratory Staff Provide a list of technical personnel which includes qualification designations (e.g. MT MLT etc.). Designate the individual s primary specialty area if this application is for more than oe specialty area.n 4.

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  • What Are IQ OQ and PQ and Why Are They Required In

     · OQ is Operational Qualification and PQ is Performance Qualification. Before you even get to IQ OQ PQ if you re acquiring a new piece of equipment you ll need design specifications that define exactly what s in that piece of equipment. Everything from the type of power source it will utilize to the exact materials used in its construction.

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  • Clinical Laboratory Program Mass.gov

     · The Clinical Laboratory Program oversees the state licensure of clinical laboratories in Massachusetts and works as the State Agency that administers the Clinical Laboratory Improvement Amendment (CLIA) program on behalf of the Centers for Medicare and Medicaid Services (CMS) for the federal certification of laboratories.

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