Self-study plan to improve fluency in English speaking, writing

Adaym

Involved In Discussions
#1
My Currently level of English speaking is at just below intermediate level needs significant improvement in English fluency, verb-subject agreement, vocab, phrases etc..
(For non-native English candidate)

Internet search results have countless suggestions. I thought to post this query on this forum. Appreciate if anyone (non-native) would like to share their personal experience (self-study/ combination) plan, resources, and materials, timebound, daily hours to put-in...etc.
 
Elsmar Forum Sponsor
Thread starter Similar threads Forum Replies Date
S Anyone know the self-selection study for home use medical device Other US Medical Device Regulations 2
B CCNA (Cisco Certified Network Associate) Self Study Help? Professional Certifications and Degrees 3
T ASQ CQA (Certified Quality Auditor) - Self - study help Professional Certifications and Degrees 3
S Best way to self study for ASQ CSSBB exam Professional Certifications and Degrees 6
X Seeking a handbook of MU or some material to start a self study Measurement Uncertainty (MU) 5
D Correct Frequence for Operator Self Inspection SPC Study Statistical Analysis Tools, Techniques and SPC 4
K GD&T training - Self Study vs. Undergrad GD&T course Training - Internal, External, Online and Distance Learning 13
C Self study training courses ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 6
M Online/self-paced ASQ CRE Exam Prep Reliability Analysis - Predictions, Testing and Standards 1
H Is CE valid in Switzerland for self certified products? CE Marking (Conformité Européene) / CB Scheme 5
R EUDAMED - IVDD self-declared devices EU Medical Device Regulations 1
P Self Certified Class 1 MDR 2017/745 Design Change CE Marking (Conformité Européene) / CB Scheme 2
Z COVID-19 Antigen Test Kit (Self-test) Registration in Peru Other Medical Device Regulations World-Wide 0
F Self Evident Inspection Method ISO 13485:2016 - Medical Device Quality Management Systems 11
F Self-test minimum requirements IEC 60601 - Medical Electrical Equipment Safety Standards Series 5
D Question and advice for a supplier self audit questionnaire ISO 13485:2016 - Medical Device Quality Management Systems 6
F Medical cart self certification EU Medical Device Regulations 1
M IATF 16949 SI # 10: Integrated self-calibration of measurement equipment- Needs for explanation IATF 16949 - Automotive Quality Systems Standard 2
K Technical file for MHRA - looking for assistance with self declaration Class I device CE Marking (Conformité Européene) / CB Scheme 8
A Self-training or Self-studying ISO 13485:2016 - Medical Device Quality Management Systems 8
K MDR Class 1 Self Certification - Competent Authority or Notified Body? EU Medical Device Regulations 6
M Control-self assessment Internal Auditing 5
Q Self-assessment audit information Quality Management System (QMS) Manuals 6
S User evaluation for self monitoring blood glucose test systems US Food and Drug Administration (FDA) 4
S Supplier Management ISO 13485: 2016- Which supplier needs to fill in a self assessment form? ISO 13485:2016 - Medical Device Quality Management Systems 6
E HONDA HAA QAV-1 Self Assessment General Auditing Discussions 6
T Formal Q Self Assessment - Problem with assigning Product and Process Customer and Company Specific Requirements 1
G Self Assessment Audit from a new potential customer General Auditing Discussions 3
M CE self-certification for Class I device (face mask) EU Medical Device Regulations 9
M Informational US FDA – Ear, Nose, and Throat Devices; Classification of the Self-Fitting Air-Conduction Hearing Aid Medical Device and FDA Regulations and Standards News 0
K Intended Use-Class I Self Certified - Intended Use and Indications for Use statements EU Medical Device Regulations 1
Ed Panek Part 11 Self Certify Memo - What else should it cover? Qualification and Validation (including 21 CFR Part 11) 5
M Informational TGA Consultation: Review of the regulation of certain self-testing IVDs in Australia Medical Device and FDA Regulations and Standards News 0
J Good Documentation Practices Self Test? ISO 13485:2016 - Medical Device Quality Management Systems 6
C CE marking for general IVD (self-certified) & ISO 13485 QMS requirements - auditing EU Medical Device Regulations 7
MichaelDRoach Oganization's Self Declaration of Conformance to ISO 28000 wording example wanted Supply Chain Security Management Systems 1
M Medical Device News TGA – Regulator Performance Framework: Self-assessment Report, July 2017 to June 2018 Medical Device and FDA Regulations and Standards News 0
A Selling CE marked self-test in Malta - any additional requirements? EU Medical Device Regulations 0
M CE self-certify, or needs testing by 3rd party? CE Marking (Conformité Européene) / CB Scheme 12
M Notified Body Involvement with Self Declared Products EU Medical Device Regulations 7
S Help: Need Control Self Assessment Questionnaire for HR Departmental Functions Process Audits and Layered Process Audits 0
T IVD - Self Declaration - Technical File - Template wanted Various Other Specifications, Standards, and related Requirements 12
R Documenting Self-Training and Effectiveness - ISO 13485:2016 Training - Internal, External, Online and Distance Learning 4
K ISO 13485:2016 Self Certification for Class I (annex 9) Stand-Alone Software? ISO 13485:2016 - Medical Device Quality Management Systems 3
S ISO9001:2015 and ISO14001:2015 Readiness/Self Evaluation Checklists wanted ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 2
N MDD Class I Medical Device Self Declaration Articles/Supplementary Documents EU Medical Device Regulations 1
Crusader Interval for Self-Calibrating Measurement Device? Calibration Frequency (Interval) 15
T Transition Time for Self Declared IVDs EU Medical Device Regulations 3
Z IVD Self Test Pregnancy - Assessment Route? EU Medical Device Regulations 5
D Off-Label Self Promotion - What to do EU Medical Device Regulations 3

Similar threads

Top Bottom