Literature Review (marketing etc)

jkc3usc

Involved In Discussions
#1
Does anyone have an example of a procedure or work instructions for literature being reviewed? Maybe the use of a checklist to show review?

Thanks
 
Elsmar Forum Sponsor
Thread starter Similar threads Forum Replies Date
A Literature review/HACCP validation of metal detection Food Safety - ISO 22000, HACCP (21 CFR 120) 0
M Informational US FDA paper – Epidemiological Evidence on the Adverse Health Effects Reports in Relation to Mercury from Dental Amalgam: Systematic Literature Review Medical Device and FDA Regulations and Standards News 0
N Proving a Medical Device is equivalent to another device from Literature Review EU Medical Device Regulations 4
A Purchasing Controls on Change Management of Literature/Labeling ISO 13485:2016 - Medical Device Quality Management Systems 3
M MDR Literature search timeline EU Medical Device Regulations 13
M Informational Grey literature and medical devices Medical Device and FDA Regulations and Standards News 0
Watchcat CERs Literature Databases - Searching for data to evaluate EU Medical Device Regulations 16
W Literature used in the clinical evaluation ISO 13485:2016 - Medical Device Quality Management Systems 4
J CER - Literature search strategy and PMV data Timeline - MEDDEV 2.7.1/ Rev 4 CE Marking (Conformité Européene) / CB Scheme 2
SK13485 Can a literature alone be used for the purpose of Clinical Evaluation of a device? EU Medical Device Regulations 6
H CER - Considering similar device/other medical devices for as relevant literature CE Marking (Conformité Européene) / CB Scheme 4
M Clinical Evaluation - MEDDEV 2.7/1 rev4 - Literature route Other Medical Device Related Standards 2
S Literature Search - Notified Body Had Questions About our Rationale CE Marking (Conformité Européene) / CB Scheme 9
K Non-Normal Data Analysis Literature, Websites, Books for Learning Quality Tools, Improvement and Analysis 2
R IQ/OQ/PQ Literature - Learning and implementing IQ/OQ/PQ procedures at my facility Design and Development of Products and Processes 3
A Finding Literature References for Clinical Evaluations per Annex X of MDD 93/42/EEU EU Medical Device Regulations 2
A Quitting ISO 9001:2000 - Necessary Changes to product literature, logos, etc. ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 14
Q Books / Literature: Risk Management for Medical Device Software recommendations Other Medical Device and Orthopedic Related Topics 4
S Clinical Evaluation using the Literature Method - Example or information wanted EU Medical Device Regulations 26
D FDA CGMP's Training Material - Slides, literature, handouts, etc. Training - Internal, External, Online and Distance Learning 1
S How do you let customers know you are certified on your literature? ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 7
R ISO 10993 - Required Testing - Can I follow the literature route? ISO 13485:2016 - Medical Device Quality Management Systems 3
Marc Liberating Scholarly Literature with E-Prints and Open Access Journals Book, Video, Blog and Web Site Reviews and Recommendations 0
L How many registrars require the use of their name in company literature Registrars and Notified Bodies 11
L Clinical Data Report - Literature Route - MEDDEV guidance (MEDDEV 2.7.1) EU Medical Device Regulations 28
I Seeking: References for online literature about ISO/TS Implementation Book, Video, Blog and Web Site Reviews and Recommendations 1
C What literature is available on Preventive Action? Book, Video, Blog and Web Site Reviews and Recommendations 7
D Control of Point of Sale Literature Document Control Systems, Procedures, Forms and Templates 3
A Document Review and Document Approval --- 2 Signatures needed acc. §820.40? 21 CFR Part 820 - US FDA Quality System Regulations (QSR) 3
Y Procedures on Contract Review Document Control Systems, Procedures, Forms and Templates 3
J Example of a defined procedure for carrying out Material Review Board (MRB) Manufacturing and Related Processes 0
A API Monogram audit review process Oil and Gas Industry Standards and Regulations 4
S Transitional Adolescent A and B - "CDRH PREMARKET REVIEW SUBMISSION COVER SHEET FORM FDA 3514" Medical Device and FDA Regulations and Standards News 1
S Risk Management Review ISO 14971 - Medical Device Risk Management 4
G Management Review (integrated system) Management Review Meetings and related Processes 17
M Management review check-list Management Review Meetings and related Processes 3
A Ethics Committee Review Process for IVD Products EU Medical Device Regulations 2
N Example for design and development planning,input,output,review,verification,validation and transfer Misc. Quality Assurance and Business Systems Related Topics 4
G Control Plan & PFMEA Review Procedure? FMEA and Control Plans 1
B SAP Audit trail Periodic Review EU Medical Device Regulations 1
K AS9100D 8.2.1 Review Requirements for Products and Services AS9100, IAQG, NADCAP and Aerospace related Standards and Requirements 14
R MRB (Material Review Board) Process using MS Sharepoint or MS Teams Manufacturing and Related Processes 2
K 510k FDA review, will they accept Biocompatibility result generated using feasibility product lots? 21 CFR Part 820 - US FDA Quality System Regulations (QSR) 8
R MDR & depth of technical files review by NB's EU Medical Device Regulations 18
D Legacy Device Review CE Marking (Conformité Européene) / CB Scheme 1
Q PPT used as Design Review ISO 13485:2016 - Medical Device Quality Management Systems 3
bryan willemot Contract Review and risk managment AS9100, IAQG, NADCAP and Aerospace related Standards and Requirements 2
J Can signed agreements over-ride review of every "contract" under ISO 13485:2016? ISO 13485:2016 - Medical Device Quality Management Systems 2
S ISO 9001 Clause 8.2.3 - Review of the requirements for products and services in a Cafe ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 8
A 510(k) review timeline 21 CFR Part 820 - US FDA Quality System Regulations (QSR) 5

Similar threads

Top Bottom