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5 whys (problem solving method) 8d problem solving 21 cfr part 11 - electronic records and signatures 21 cfr part 111 - dietary supplements (misc) 21 cfr part 807 - establishment registra. & device listing 21 cfr part 812 - investigational device exemptions 21 cfr part 820 - med. device mfger. qsr requirements 510(k) 510(k) exempt device 2017 2018 2020 accelerated life and stability testing acceptance criteria accreditation bodies accuracy (general term) accuracy of a measurement device acronyms active medical device adverse event reporting aea - aerospace experience auditor aerospace (general) aerospace standards and regulations aiag (automotive industry action group) aiag manual(s) alarms (visual and/or audible) aluminum (general topics) amdd - asean medical device directive ams 2750 - pyrometric requirements anab (ansi-asq national accreditation board) andons animal studies annex ii annex x annual layout inspection anova (analysis of variance) ansi y14.5 - dimensioning and tolerancing ansi z1.4 - inspection by attributes api (american petroleum institute) api q1 - oil industry quality management system (qms) app (mobile device software) applicable clauses documents legal requirements etc. approvals approved supplier list (asl) apqp (advanced product quality planning) aql (acceptable quality level) as9100 - aerospace quality management systems as9100 revision d (2016) as9102 - aerospace first article inspection (fai) as9104 - aerospace qms registration requirements as9110 - aerospace maintenance quality systems as9120 - aerospace qms requirements for distributors as9146 (foreign object damage (fod) prevention program) aspects and impacts (environmental) 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 auditing remote locations audit man-days audit nonconformances and findings audit observation auditor qualification requirements and certifications auditors (general topics) auditor training audit plans and audit frequency audit questions audit reports audits and auditing audit scope australia tga authorized representative autoclaves automotive (general) automotive industry barcoding (upca - upce - ean8 - ean 13 - qr code) batch manufacturing (general) batch manufacturing records batch production battery (electric batteries) battery powered devices benefit(s) best practices bias study (measurement) bioburden biocompatibility biocompatibility requirements biocompatibility testing boeing books brazil brochures business processes business process maps cables (electrical and related such as signal carriers) cables (general) calibration (general topics) calibration (metrology) laboratories calibration data calibration interval (aka frequency) calibration of shop tools calibration past due date measurement equipment and gages calibration procedures and methods calibration reports and certificates calibration verification calipers canada canned procedure(s) and documentation capa (corrective and preventive action) capability study (part dimensions from a process or machine) career changes 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 certificate (content) certification process certifications (professional) certifications (to a standard) certified calibration technician (cct) cfda (china food and drugs administration) cgk change(s) (general) change control change management change notice (process or product) aka pcn charts checklist or check sheet china class i exempt medical device 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 data management (cdm) clinical evaluations and reports clinical research clinical trials and studies and investigations cloud computing cmk cmm (coordinate measuring machine) cnc machine shop cnc machining coatings cofepris (mexico's medical device and ivd oversight) combination devices and related rules combination drug-device products communications community discussions company name change company policies comparison matrix competence assessments competency complaint files and reports complaint handling process complaints (general) compliance (general) compliance to a standard components concessions conformity assessment bodies conformity assessments 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 research organizations (cro) contract review and approval contracts and agreements (general) contract services control charts (general) control chart software controlled documents control limits control methods control of production equipment control plans controls convenience kits (medical device) copyrights corrective action (ca) corrective action request (car) corrective action systems cots (commercial off-the-shelf) counterfeiting control counterfeit parts and products cpk (related to process capability) cqe (certified quality engineer) cqe exam cqi 9 - heat treat cqi 23 - molding system assessment cqi requirements (customer specific requirements) creepage distance critical characteristics critical parts and components critical processes (general) critical suppliers cross reference matrix customer approval customer communication customer complaints and customer found nonconformance customer feedback customer requirements customer service 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 dates (general) datum (gd&t) datum feature references dcma (defense contract management agency) declaration of conformity definitions delivery of products and services dental topics design and development design and engineering control design changes design control design engineering company design exclusion design history file (dhf) design history record (dhr) design inputs and outputs design master records (dmr) design of experiments (doe) design validation design verification design verification testing (dvt - medical devices) deviations from a print or requirement device master record (dmr) dfars (defense federal acquisition regulation supplement) dfmea (design fmea) diagnostic devices (medical) diameter measurement dielectric strength dies differences (general) dimensional inspection dimensions displays (video monitors) disposable products 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 revisions and changes documents and documentation (general) documents of external origin dod (department of defense) dosimeter drawing (also see prints) drug master file (dmf) drugs (medicinal) easa (european aviation safety agency) easa part - 145 maintenance organisation approval effectiveness efficiency electrical safety electromagnetic compatibility 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) emc (electromagnetic compatibility) employee awareness employee development and motivation employees (general) employee training and qualifications employee turnover endoscopic equipment engineering change order (eco) engineering change request (ecr) engineering changes engineering company engineering drawings epoxy (general) equipment qualification and validation equivalent medical devices error proofing escalation process essential performance essential requirements checklist etl (intertek's edison testing laboratories) eto (ethylene oxide) sterilization eu 2017/745 europe european medical device regulations european union european union medical device directives (mdd) european union regulations and standards evidence exclusions of clauses in a standard exclusions of product lines in registration to a standard expiration date exports and exporting external audits and auditors external communications external document control external documents - prints standards etc. external issues external processes external services faa (federal aviation administration) faa part 145 (certified repair station) faa regulations and requirements faa repair stations failure modes fda (food and drug administration) fda guidance fda news fda requirements feedback final inspection and/or testing financial (finance) departments first article inspection (fai) first article inspection report (fair) fishbone diagram flowcharts fmea - failure modes and effects analysis 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 suggestions (general) fraud furls (fda's electronic registration and listing system) gage blocks gage r&r (repeatability and reproducibility) gages (measurement and monitoring devices) gamma irradiation sterilization gamp (good automated manufacturing practice) gamp validation procedures gap analysis gd&t (geometric dimensioning & tolerancing) gdp (good documentation practices) gdpr (eu general data protection regulation) general motors (gm) germany glp (good laboratory practices) gmdn (global medical device nomenclature) gmp (good manufacturing practices) go no-go gage gs1-128 barcodes gtin (global trade item number) gudid (fda global udi database) guidance documents hardness measurement harmonization of standards hazard identification and risk assessment health (general) health canada heat treatment hipaa (health insurance portability and accountability act) histogram history home healthcare hospital use humidity control humor iaf (international accreditation forum) iaqg (international aerospace quality group) 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 iec 62366 - medical device usability engineering iec 62366-1:2015 medical device usability imdrf (international medical devices regulators forum) imds (international material data system) implantable medical devices (imd) implementation of a standard in a company implementing iatf 16949 implementing iso 9001 imports and importation improvement improvement plans and projects in-house calibration in-process inspection incoming inspection (also see receiving inspection) india information security information technology (it) department infrastructure injection medical devices injection molding innovation inputs (general) inspection (general) inspection devices tools and fixtures inspection methods and plans inspection records inspectors 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 interpretations interviews and interview questions ishikawa diagram isms (information security management system) iso (int'l organization for standardization) iso 2859 - sampling for inspection by attributes iso 9001 - quality management systems iso 9001:2015 iso 10993 - biological evaluation of medical devices iso 11137 - medical device radiation 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 15223 - medical device label symbols iso 17020 - criteria for bodies performing inspection iso 17025 - testing and calibration laboratories iso 19011 - quality (qms) and ems audits iso 26000 - social responsibility iso 27001 - information security management system (isms) iso 31010 - risk assessment techniques iso 45001 - occupational health and safety management standard iso 62366 - medical device usability engineering israel ivd (in vitro diagnostic) devices and reagens ivdd ivdr (in vitro diagnostic regulations) j-std-001 japan job openings jobs (general) 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 layout inspection lead auditor(s) and related topics lead auditor course leadership leakage current leak tester lean lean six sigma leed environmental building program legacy products legal requirements life cycle of a device or product linkedin lithium ion batteries low voltage directive 2006/95/ec machine shop machining processes maintainability maintenance malaysia management management representative management review manuals (misc) manufacturing (general term) manufacturing location change manufacturing planning manufacturing processes marketing (general) mathematical equations matrix mdd (medical device directive) mdd 93/42/eec mdr (medical device regulations) mdr (medical device reporting) mdr 745/2017 mds (material declaration sheet) mdsap (medical device single audit program) mds reporting mdvr - medical device vigilance report measureables (also see metrics) measurement (general) measurement and monitoring and test devices measurement equipment resolution and tolerances measurement equipment verification measurement systems measurement techniques and procedures measurement uncertainty (mu) medaccred industry program meddev - ec guidelines on medical devices medical device accessories medical device company or industry medical device data systems 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) metal forming and stamping method validation metrics (measurables such as for objectives) mhlw (japan's ministry of health labor and welfare) mhra (medical & healthcare regulatory agency) microbial count micrometers microsoft excel .xls .xlsx spreadsheet microsoft sharepoint software minimum requirements minitab (statistical analysis software) mmc (maximum material condition - gd&t) 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 music nadcap (nat'l aerospace & defense contractors accred. pgm) nadcap ac7108 nadcap ac7114 ndt (non-destructive test) new products and new product requirements news 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 nrtl (nationally recognized testing laboratories) nuclear (general) oasis (online aerospace supplier information system) oasis database objective evidence 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 ojt - on the job training (also see training) online internet training courses and universities operational control operational qualification (oq) operator instructions opportunities (general) opportunities for improvement (ofi) optical comparators order processing organizational knowledge organization structure orthopedic implants orthopedics (general topics) otc (over the counter) pharmaceuticals outputs (general) outsourced products and processes outsourced software outsourcing ovens packaging (general) packaging labeling and related requirements packaging sealing packaging standards and specifications painted surfaces paper documents and records pcb (printed circuit board) pdca cycle (plan do check act) pear (process effectiveness assessment report) pems (programmable electrical medical system) performance evaluation studies (medical devices) performance measureables performance qualification (pq) performance testing personal health information pfmea (process fmea) pharmaceuticals and pharmaceutical industry pin gages plastic extrusion plastic injection molding plastic parts plastics plating & coatings pma (pre-market approval) pmda (japan) policies and policy statements policy documents post market activities (misc) post market clinical follow up post market surveillance ppap (production part approval process) ppap review and approval ppk (related to process performance) ppm (parts per million) pre-control chart premarket review process premarket submissions presentations pressure (general) pressure gages preventive action (pa) preventive maintenance print (drawing) callouts prints (drawings or blueprints) private label manufacturer private label products 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 production line production processes product lifecycle management (plm) product limits product realization product safety products and services professional associations professional certifications and degrees profile of a surface project management promotional materials prototypes and prototype testing purchase orders purchasing purchasing controls purchasing department qms (quality management system) qualification of equipment and processes quality quality assurance (qa) quality control (qc) quality control data quality department quality engineer(s) quality management systems quality manuals (general) quality manuals - structure contents and examples quality objectives quality plans and quality planning quality policy quality records quality systems quality tools quotes (quotations for a service or product) 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 documents reference standards refurbishing registrar audits registrar ratings and reviews registrars (registration bodies) registration audits registration requirements registration to a standard registration to multiple standards regression analysis (statistical technique) regrind material regulations and regulatory requirements regulatory affairs (ra) 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 thesis research use only (ruo) device or software reselling resistance (electrical) resources response time responsibilities returned products and/or parts reusable medical devices revision control revisions to a document or standard rework rework and repair procedures 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) root cause failure analysis rta (refuse to accept) guidance rubber part or material run at rate russia s-charts safety (general) safety requirements and regulations sai salt spray testing samples (of a part product or service) samples (of a product or service for customer evaluation) samples and sampling plans sample size sampling plans for attribute data sanctioned interpretations sap erp (enterprise resource planning) saudi arabia scales and balances 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 certification sequence and interactions of processes service company or industry service providers service provisions severity ranking (fmea) shelf life shipping (general) and shipping requirements signatures single use devices (sud) six sigma (general) small companies (small businesses) software (general topics) software (off the shelf) software development life cycle (sdlc) software medical devices software quality assurance software tools (for qa statistics doc control etc.) software validation soldering sop (standard operating procedure) sorting out nonconforming material or goods spain spanish spare parts spc (statistical process control) special characteristics special processes specification details specifications (general term) sri lanka stability testing stage 1 assessment stainless steel stakeholders in a company stamps (e.g. inked document control 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 sterile packaging sterility and sterilization techniques sterilization (general) sterilization validation storage (general) storage requirements and specifications strategic planning and objectives student questions sub-supplier subcontracting and subcontractors supplier supplier audits supplier control and monitoring supplier corrective & preventive action supplier development supplier evaluation/rating/approval supplier nonconformances supplier performance supplier requirements suppliers (general topics) supplier selection qualification and approval support processes surgery products surgical products surveillance audits surveys (general) swot (strengths weaknesses opportunities and threats) symbolization for devices symbols (general) taguchi designs and analysis tape measure targets (aka objectives) tc 176 (iso technical committee for iso 9000 documents) technical documentation technical files for medical devices templates tensile strength and tensile strength testing test equipment testing (general testing topics) testing laboratories test methods and procedures and plans test reports texas tga (therapeutic goods administration) third party audits and auditing thread plug gages and set plugs thread ring gages and setting plugs threads (of fasteners such as nuts and bolts) tolerances (dimensional or other units) tooling control top management torque wrench or tool toyota tpm - total productive maintenance tqm (total quality management) traceability (misc) traceability of calibration (measurement) standards traceability of parts materials and products training (general) training (on-the-job) training effectiveness training materials training records training requirements training sources and resources transfer (general) transition (between standards or revisions to a standard) transition audits transition period translations (languages) true position ts 16949 - automotive quality system standard turtle diagrams tus (temperature uniformity survey) uae (united arab emirates) ukas (united kingdom accreditation service) ultrasonic testing uncertainty (aka mu - related to calibration) uncertainty budget (measurement) unique device identification (udi) united kingdom (uk) upper management usability of a product usb port isolation validation (general) validation of machines equipment processes design etc. validation plan validation requirements validation testing value stream mapping (vsm) variables data vda 6.3 - process audit vda standards verification (general) verification of calibration verification testing version changes and change control virtual manufacturing vision measurement systems (electronic) visual inspection want to buy warehouse (general) webinar websites weee (waste electrical and electronic equipment) weekend random topics welding wire wire harnesses work environment work instructions (wi) x-bar & r chart zero defects

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