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5s workplace organization methodology 7.5.4 - customer property 7.6 - control of monitoring & measurement devices 8d problem solving 21 cfr part 11 - electronic records and signatures 21 cfr part 211 - finished pharmaceuticals cgmp 21 cfr part 801 - labeling 21 cfr part 812 - investigational device exemptions 21 cfr part 820 - med. device mfger. qsr requirements 510(k) 510(k) exempt device 2016 2017 2018 accelerated life and stability testing acceptance criteria accessories (product) accreditation bodies accuracy of a measurement device acquisitions and mergers acronyms active medical device adverse event reporting aea - aerospace experience auditor aerospace (general) aerospace auditor aerospace standards and regulations aiag (automotive industry action group) aiag manual(s) alarp (as low as reasonably possible) aluminum (general topics) amdd - asean medical device directive ams 2750 - pyrometric requirements anab (ansi-asq national accreditation board) annex v/vii annex x anova (analysis of variance) ansi y14.5 - dimensioning and tolerancing ansi z1.4 - inspection by attributes anvisa api (active pharmaceutical ingredients) api (american petroleum institute) api q1 - oil industry quality management system (qms) app (mobile device software) applicable clauses documents legal requirements etc. approvals apqp (advanced product quality planning) aql (acceptable quality level) article 12 as9100 - aerospace quality management systems as9100 revision d (2016) as9101 - aerospace qms audit requirements as9102 - aerospace first article inspection (fai) as9110 - aerospace maintenance quality systems as9120 - aerospace qms requirements for distributors asl (approved supplier list) asq (american society for quality) asq certifications assembly (a "unit" made up of various parts) assembly (general term) astm (american society for testing and materials) attribute data attribute data msa (measurement system analysis) audit checklist audit man-days audit nonconformances and findings audit observation auditor performance auditor qualification requirements and certifications auditor reporting auditors (general topics) auditor training audit plans and audit frequency audit questions audit reports audits and auditing audit scope australia australia tga authority and responsibility authorized representative autoclaves automotive (general) automotive industry aws (american welding society) barcoding (upca - upce - ean8 - ean 13 - qr code) batch manufacturing (general) batch manufacturing records batch production battery (electric batteries) battery powered devices benefit(s) bill of materials (bom) bioburden biocompatibility biocompatibility requirements biocompatibility testing birthdays blood glucose meters and test strips boeing books brazil bribes brochures business development business processes cables (general) calculation formulas calibration (general topics) calibration (metrology) laboratories calibration data calibration interval (aka frequency) calibration procedures and methods calibration reports and certificates calibration verification calipers canada canadian medical devices capa (corrective and preventive action) capability study (part dimensions from a process or machine) careers catheters cba (certified biomedical auditor) cba (certified biomedical auditor) exam cdrh (center for devices and radiological health) ce mark and ce marking certificate of conformance (c of c) certificate of free sale certificates (general) certification audits certification bodies (cb) certification process certifications (professional) certifications (to a standard) certified calibration technician (cct) cfda (china food and drugs administration) change(s) (general) change control change management change notice (document or form) charts checklist or check sheet china chrysler classification(s) of parts or products class iii medical device class ii medical device class i medical device cleaning methods and processes cleaning validation cleanliness cleanrooms clinical evaluations and reports clinical trials and studies and investigations cloud computing cmdcas (canadian med device conformity assmnt system) cmk cmm (coordinate measuring machine) cnc machine shop cnc machining coatings cofepris (mexico's medical device and ivd oversight) color measurement combination devices and related rules combination drug-device products communications community discussions company name change company organization company policies company vision or strategy comparison matrix competence assessments competency complaint files and reports complaint handling process complaints (general) compliance (general) compliance to a standard component manufacturers components concessions connectors (electrical) construction company or industry consultants and consulting containment (related to nonconformances) contamination (also see fod - foreign object damage) context of the organization contingency plans continual improvement (also see continuous improvement) continuous improvement continuous process(es) contract audits and contract auditing contract manufacturing contract review and approval contracts and agreements (general) control charts (general) controlled documents control limits control methods control plans controls convenience kits (medical device) conversion factors copyrights corrective action (ca) corrective action request (car) corrective action systems cost estimation cots (commercial off-the-shelf) counterfeiting control counterfeit parts and products country specific standards and regulations cpk (related to process capability) cqa (certified quality auditor) cqe (certified quality engineer) cqe exam cqi 23 - molding system assessment creepage distance critical characteristics critical parts and components critical suppliers crossed gage r&r customer approval customer communication customer complaints and customer found nonconformance customer owned property customer property customer requirements customer satisfaction customer specific requirements (csr) cycle time data (general) data (import from and export to applications) data analysis databases data collection and/or entry data control data integrity data security date of manufacture datum (gd&t) datum feature references dcma (defense contract management agency) deaths declaration of conformity defect rate defects and defectives definitions dental topics design and development design changes design control design exclusion design history file (dhf) design history record (dhr) design inputs and outputs design of experiments (doe) design validation design verification destructive tests and testing detection ranking (fmea) deviations from a print or requirement device history file (dhf) device history record (dhr) device master file device master record (dmr) dfars (defense federal acquisition regulation supplement) dfmea (design fmea) diameter measurement dielectric strength differences (general) dimensions displays (video monitors) distribution centers distribution of products distributors (distribution company) distributors (general) distributors (medical devices) dock audits dock to stock document content & structure document control document control (electronic) document control software documented procedures (requirements for) document identification and numbering document references document retention document review(s) and approval(s) document revisions and changes documents and documentation (general) documents of external origin dod (department of defense) dose audit dosimeter draft documents drawing (also see prints) drug devices drug master file (dmf) drugs (medicinal) easa (european aviation safety agency) easa part - 145 maintenance organisation approval education effectiveness efficiency electrical safety electrocardiographs (general topics) electronic components parts assemblies and products electronic documents forms and templates electronic records electronic signatures and approvals elsmar elsmar cove tos and policies elsmar improvements (general) email (general) emc (electromagnetic compatibility) employee awareness employee development and motivation employees (general) employee training and qualifications ems (environmental management system) endoscopic equipment energy use and conservation engineering change request (ecr) engineering changes engineering drawings environment (environmental related) epoxy (general) equipment qualification and validation equivalent medical devices erp software essential requirements checklist ethylene oxide (eo) etl (intertek's edison testing laboratories) eto (ethylene oxide) sterilization eu 2017/745 european medical device regulations european union european union regulations and standards evidence evop (evolutionary operation of processes) examinations (course or certification tests) exclusions of clauses in a standard exemptions expiration date exports and exporting external audits and auditors external communications external document control external documents - prints standards etc. external laboratories (including calibration and testing) external processes faa (federal aviation administration) faa part 145 (certified repair station) faa repair stations failure modes fda (food and drug administration) fda guidance fda requirements feedback final inspection and/or testing firmware first article inspection (fai) first article inspection report (fair) first piece approval flammability flowcharts fmea - failure modes and effects analysis fmea manual fmea rankings fod (foreign objects and debris) food (general) food safety ford motor company ford q1 foreign manufacturing formats and formatting forms and templates (general) formula (mathematics/statistics) for sale forum software (general) forum software instructions forum software problems forum software questions forum suggestions (general) fraud functional requirements furls (fda's electronic registration and listing system) gage blocks gage r&r (repeatability and reproducibility) gages (measurement and monitoring devices) gamma irradiation sterilization gamma sterilization gamp (good automated manufacturing practice) gap analysis gd&t (geometric dimensioning & tolerancing) gdpr (eu general data protection regulation) general motors (gm) gmp (good manufacturing practices) goals (quality environmental and other measureables) go no-go gage gp-12 early production containment gs1-128 barcodes gtin (global trade item number) gudid (fda global udi database) gui (graphic user interface) guidance documents hardness measurement harmonization of standards hazard analysis hazard identification and risk assessment health (general) health canada health safety and environmental (hse) heat treatment hipaa (health insurance portability and accountability act) history holes in parts - location(s) holidays and related occasions home healthcare hospitals human factors human tissues and organs humidity (general) humidity control humidity testing humor hypothesis test analysis iaf (international accreditation forum) iaqg (international aerospace quality group) iaqg 9100:2016 - aerospace quality management systems iatf (international automotive task force) iatf 16949:2016 identification (products and parts etc) identification and traceability (general) iec 60335 - household electrical appliance safety iec 60601 - medical electrical equipment iec 60950 (information technology equipment - safety) iec 61010 - safety requirements for electrical equipment iec 62133 - secondary cells and batteries safety requirements iec 62304 - medical device software life cycle processes imds (international material data system) implantable medical devices (imd) implementation of a standard in a company implementing a qms implementing iatf 16949 implementing iso 9001 imports and importation improvement improvement plans and projects in-process inspection incoming inspection (also see receiving inspection) india indian health ministry information security information technology (it) information technology (it) department infrastructure infusion pumps and devices injection molding inputs (general) inspection (general) inspection devices tools and fixtures inspection methods and plans inspection records installation qualification (iq) instructions for use (ifu) integrated management systems interaction of processes (see process interactions) interested parties internal auditors internal auditor training internal audits internal issues internal laboratory international standards internet (general topics and news) interpretations iran ishikawa diagram isms (information security management system) iso (int'l organization for standardization) iso 9001 - quality management systems iso 9001:2015 iso 10993 - biological evaluation of medical devices iso 11135 - medical device ethylene oxide sterilization iso 13485 - medical device qms iso 13485:2016 iso 14001 - environmental management systems iso 14001:2015 iso 14155 - good clinical investigation practices iso 14644 - cleanrooms and controlled environments iso 14971 - medical device risk management iso 15197 - in vitro glucose monitoring systems iso 15378 - primary packaging materials for medicinal products iso 16269 - statistical interpretation of data iso 17025 - testing and calibration laboratories iso 19011 - quality (qms) and ems audits iso 22000 - food safety management systems iso 26000 - social responsibility iso 27000 series - information technology security iso 27001 - information security management system (isms) iso 31000 - risk management iso 31010 - risk assessment techniques iso 45001 - occupational health and safety management standard iso 62366 - medical device usability engineering isolation israel itar (international traffic in arms regulations) ivd (in vitro diagnostic) devices and reagens ivdd ivdr (in vitro diagnostic regulations) j-std-001 japan japanese pharmaceutical and medical device act job descriptions job openings jobs (general) kaizen key performance indicators (kpi) knowledge management korea kpi data labeling - eu labeling directive labeling content labeling requirements labels and labeling (general) label symbols laboratories (general) laboratory scope language requirements layered process audit (lpa) layout inspection lead auditor course leadership leakage current leak test lean lean manufacturing lean six sigma leed environmental building program legacy products legal requirements level of concern (fda term) life cycle of a device or product listing number lithium ion batteries load cells low voltage directive 2006/95/ec low volume production machine shop machining processes maintenance malaysia management management representative management review manufacturing processes marketing (general) marking (general such as labeling) mathematical equations matrix maude database of fda medical device reports mdd (medical device directive) mdd 93/42/eec mdr (medical device regulations) mdr (medical device reporting) mds (material declaration sheet) mdsap (medical device single audit program) mds reporting measureables (also see metrics) measurement (general) measurement and monitoring and test devices measurement equipment resolution and tolerances measurement systems measurement techniques and procedures measurement uncertainty (mu) meddev - ec guidelines on medical devices medical device accessories medical device company or industry medical device electronics and electrical equipment medical device file medical device licensing medical device listing codes and classifications medical device parts and components medical device registration medical device repair and servicing medical device reports including incident reporting medical devices medical devices (disposable) medical device safety medical device software medical device standards and regulations medical equipment (general) medwatch (fda safety info & adverse event reporting system) metal forming and stamping method validation metrics (measurables such as for objectives) mexico mhlw (japan's ministry of health labor and welfare) mhra (medical & healthcare regulatory agency) micrometers microsoft excel .xls .xlsx spreadsheet microsoft sharepoint software minitab (statistical analysis software) mmc (maximum material condition - gd&t) mobile medical devices and applications (apps) monitoring monitoring and measurement moop (means of operator protection) mop (means of protection) mopp (means of patient protection) mra (mutual recognition agreement- tga australia and eu) msa (measurement system analysis) msa manual msa study msds (material safety data sheet) multiple business units multiple national or international locations multiple sites multiple standards in a company nace codes nadcap (nat'l aerospace & defense contractors accred. pgm) nadcap ac7114 navistar nested gage r&r new products and new product requirements news nhs (uk national health service) nist (nat'l institute of standards & technology) non-normal data distribution non-sterile medical devices nonconformance recurrence nonconformance report (ncr) nonconformances nonconformance system nonconforming material product or service notified bodies medical devices (nb-med) notified body nylon oasis (online aerospace supplier information system) oasis database objectives (quality environmental and other measureables) obl (own brand labeling) occupational health and safety (oh&s) occurrence ranking (fmea) oem (original equipment manufacturer) off the shelf (ots) equipment or parts or software ohsas 18000 & 18001 & 18002 online internet training courses and universities operational control operational planning operational qualification (oq) opportunities (general) opportunities for improvement (ofi) order processing organization organizational knowledge orthopedic implants osha (occupational safety and health admin) outputs (general) outsourced products and processes outsourcing ovens packaging (general) packaging labeling and related requirements packaging standards and specifications painting paper documents and records particulates part numbering pcb (printed circuit board) pear (process effectiveness assessment report) pems (programmable electrical medical system) peppol (pan-european public procurement online) performance measureables performance qualification (pq) performance testing personal health information pfmea (process fmea) pharmaceuticals and pharmaceutical industry philippines planning plastic injection molding plastic parts plastics plating & coatings pma (pre-market approval) pmda (japan) poka yoke policies and policy statements policy documents post delivery activities post market clinical follow up post market surveillance ppap (production part approval process) ppk (related to process performance) ppm (parts per million) premarket approval premarket notification premarket submissions presentations pressure gages preventive action (pa) preventive maintenance print (drawing) callouts prints (drawings or blueprints) problem solving procedure examples procedure format procedure pack (medical devices) procedures (general) process approach process audits process capability process changes and change notifications process controls and control plans process design and development processes (general) process flowcharts (process diagrams) process fmea process interactions process mapping process measurement and monitoring process performance process validation process verification and validation product audits product code production product limits product requirements product safety products and services professional certifications and degrees profile of a surface project management proprietary information prototypes and prototype testing psw (part submission warrant) purchase orders purchasing purchasing controls purchasing requirements qms (quality management system) qualification of equipment and processes quality quality assurance (qa) quality control (qc) quality control data quality department quality management systems quality management system software quality manuals (general) quality manuals - structure contents and examples quality objectives quality plans and quality planning quality policy quality records quality system manuals quality systems quality tools radius measurement raps (regulatory affairs professionals society) raw materials raw material suppliers reach (ec 1907/2006) reach rohs recalls (general) receiving inspection recertification (to a standard) record retention requirements records (evidence) and records control reference dimensions refurbishing registrars (registration bodies) registration audits registration certificate registration requirements registration to a standard regression analysis (statistical technique) regrind material regulations and regulatory requirements regulatory affairs (ra) regulatory bodies regulatory compliance regulatory requirements relabeling (of products) reliability analysis and testing remote locations and sites repackaging repair and or overhaul reports (general) required documents required procedures required processes requirements and specifications research and development (r&d) research use only (ruo) device or software resistance (electrical) resources response time responsibilities returned products and/or parts revalidation of a process or product revision control revisions to a document or standard rework rework and repair procedures rfid (radio frequency identification) ring gage risk and opportunities risk based compliance risk based thinking (rbt) risk management and analysis risk management file (rmf) risk register robotics rohs (restriction of hazardous substances) rohs 2 directive root cause failure analysis rpn (fmea risk priority number) rubber part or material russia s-charts safety (general) safety requirements and regulations salt spray testing samples (of a part product or service) samples and sampling plans sample selection (selection of samples) sample size sampling plans for attribute data sampling plans for variables data sanctioned interpretations sap erp (enterprise resource planning) saudi arabia scales and balances scar (supplier corrective action request) scope (general term) scope of accreditation scope of certification (aka registration) scope of registration/certification changes scope of the qms scrap second party audit self declaration service company or industry service providers service provisions severity ranking (fmea) shelf life shipping (general) and shipping requirements signatures single fault condition single use devices (sud) six sigma (general) small companies (small businesses) smed (single minute exchange of dies) software (general topics) software (off the shelf) software development life cycle (sdlc) software medical devices software tools (for qa statistics doc control etc.) software validation soldering sole source supplier sop (standard operating procedure) sorting out nonconforming material or goods spain spare parts spc (statistical process control) special characteristics special processes specifications (general term) spectrophotometer sri lanka stability testing stage 1 assessment stainless steel stakeholders in a company stamps (e.g. inked inspection stamps) standard deviation (stdev in statistics) standards (e.g. iso mdd ansi etc.) standards (measurement) startup business statistical analysis and studies statistical analysis tools statutory requirements sted (summary technical documents) steel plating sterile medical devices sterility and sterilization techniques sterilization (general) sterilization validation storage (general) strategic planning and objectives student questions subcontracting and subcontractors substantial equivalence supplier supplier audits supplier control and monitoring supplier corrective & preventive action supplier development supplier evaluation/rating/approval supplier nonconformances supplier performance supplier quality supplier requirements suppliers (general topics) supplier selection qualification and approval support processes surgical products surveillance audits sustainability swot (strengths weaknesses opportunities and threats) taguchi designs and analysis tape measure targets (aka objectives) taxes and taxation technical documentation technical files for medical devices temperature (general) temperature control and tolerances tensile strength and tensile strength testing terminology test equipment testing (general testing topics) testing laboratories test methods and procedures and plans test reports tga (therapeutic goods administration) thermocouples third party audits and auditing thread inspection gages thread plug gages and set plugs thread ring gages and setting plugs threads (of fasteners such as nuts and bolts) tl 9000 tolerances (dimensional or other units) tools and tooling (general) top management torque wrench or tool touch current (tc) toyota tpm - total productive maintenance traceability (misc) traceability of calibration (measurement) standards traceability of parts materials and products training (general) training effectiveness training materials training records training requirements training sources and resources transfer (general) transformer (electrical) transition (between standards or revisions to a standard) transition audits transition period translations (languages) travel true position ts 16949 - automotive quality system standard turtle diagrams ultrasonic testing uncertainty (aka mu - related to calibration) uncertainty budget (measurement) unique device identification (udi) united kingdom (uk) upper management usability of a product usp (united states pharmacopeia) validation (general) validation of machines equipment processes design etc. validation plan validation requirements validation testing variables data vda 6.3 - process audit vda standards verification (general) verification of calibration virtual manufacturing visual inspection volkswagen want to buy warehouse (general) webinar weee (waste electrical and electronic equipment) weekend random topics welding white papers wifi wireless rf transmission wire wire harnesses work instructions (wi) zero defects

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