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Guideline document for the 2023 IEEE IAS Global Mentorship Program contest, detailing eligibility, submission rules, event structure, assessment criteria, and participation requirements for local mentoring events.
Year:
2023
Organization:
IEEE Industry Applications Society (IAS)
Type of Document:
Contest guideline
Target Audience:
IEEE IAS Student Branch Chapters, IEEE Young Professional Affinity Groups
Event Period:
20 February 2023 – 20 June 2023
Submission Format:
Physical report (following Sample Report Template)
Assessment Panel:
IEEE IAS members
Eligibility Criteria:
IEEE IAS SBCs or YP Affinity Groups with active IEEE IAS members
Event Format:
In-person local mentoring events
Evaluation Criteria:
Goals and objectives, number of attendees, mentor experience, topics covered, program structure, lessons learnt
Awards:
Monetary prizes specified in Section 9
Contact Information:
Provided in Section 10
Price: 8 / 10 USD
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The product description is provided for reference. Actual content and formatting may differ slightly.
Year:
2023
Region / City:
Mauritius and Seychelles
Theme:
Environmental Management, Invasive Species, Project Evaluation
Document Type:
Management Response, Evaluation Report
Organization:
UNDP Mauritius and Seychelles CO
Author:
Seewajee Pandoo
Target Audience:
Project Management, Environmental Experts, Policy Makers
Period of Action:
June 2023
Date of Approval:
June 2023
Date of Updates:
N/A
Contextual description:
Management response to mid-term evaluation of the IAS Prevention, Control and Management project, outlining key actions and recommendations to address project implementation challenges.
Year:
2020
Event:
IEEE IAS Annual Meeting
Document Type:
Digest Guidelines / Template
Audience:
Authors submitting digests
Page Limit:
3–5 pages
Font:
12 pt, single column, 1.20–1.65 line spacing
Figures:
TIFF or EPS, 300 dpi recommended
References Style:
IEEE
Submission Requirements:
Anonymous, no author details in PDF properties
Year:
2023
Region / City:
Not specified
Subject:
Quality management system compliance
Document Type:
Checklist
Organization / Institution:
IAS
Author:
Not specified
Target Audience:
PCI-certified plants, IAS assessors
Validity Period:
Not specified
Approval Date:
Not specified
Amendment Date:
Not specified
Note:
Year
Topic:
GST, Business Activity Statements, Instalment Activity Statements
Document Type:
Assessment Workbook
Target Audience:
Students, Assessors
Year:
2019
Event:
Awards Luncheon
Organization:
IEEE IAS Petroleum and Chemical Industry Committee (PCIC)
Location:
Vancouver, Canada
Chair:
Dennis Bogh
Award Recipients:
Michael Wactor, Robert Durham, Robert Burns, Dane Martindale, Robert McElveen, Giovanni Parra, and others
Subcommittees Recognized:
Awards Nominating, Facilities Planning, Publicity, Membership, Young Engineers Development, Safety, Production, Chemical, Transportation, International
Standards Acknowledged:
IEEE 45.4, IEEE 1708-2018, IEEE/CSA 844.3, IEEE/CSA 844.4, IEC/IEEE 80005-1:2019, IEEE 1584
Target Audience:
PCIC Members, IEEE Professionals
Date of Event:
September 9, 2019
Type of Document:
Event Program / Recognition List
Year:
2013
Region / City:
Manipur
Theme:
Administrative Officers
Document Type:
List
Institution:
Government of Manipur
Author:
Not specified
Target Audience:
Public Administration Personnel
Effective Period:
As of 29/08/2013
Date of Approval:
Not specified
Date of Changes:
Not specified
Contextual description:
A list of IAS officers currently serving in various administrative roles within the Manipur region, including their assignments and year of allotment.
Year:
2016
Region / city:
Mauritius
Theme:
Biodiversity
Document Type:
Project Identification Form
Agency/Organization:
UNDP, Ministry of Agro-Industry and Food Security
Author:
UNDP
Target Audience:
Government agencies, environmental organizations
Period of Validity:
2016–ongoing
Approval Date:
July 23, 2016
Date of Amendments:
Not specified
Year:
2014
Document Type:
Government Data Table
Ministry/Department:
Rajya Sabha
Subject:
Indian Administrative Service (IAS) Cadre Strength
Scope:
All Indian States and Union Territories
Data Reference Date:
01.01.2014
Question Number:
1766
Respondent:
Shri DHIRAJ PRASAD SAHU
Positions Analyzed:
Authorized Cadre Strength, Officers in Position, Shortages
Data Source:
Annexure-I and Annexure-II
Note:
Year
Topic:
Foreign Travel
Document Type:
Checklist
Organization / Institution:
USTP System
Author:
RAMIR PHILIP JONES V. SONSONA
Target Audience:
Board of Regents
Context:
Document listing the required items for endorsement of official foreign travel requests, intended for internal administrative use.
Year:
2026-2027
Note:
Region / City
Document Type:
Form
Organization / Institution:
IEEE
Note:
Year
Topic:
Construction Management
Document Type:
Guaranteed Maximum Price (GMP) Submission
Organization / Institution:
University of Michigan
Year:
2010
Region / City:
European Union
Topic:
Good Manufacturing Practice (GMP) inspection
Document Type:
Inspection report
Organization / Institution:
European Commission, Directorate-General for Health and Food Safety
Author:
European Medicines Agency
Target Audience:
Competent Authorities, Pharmaceutical Manufacturers
Period of Validity:
From 1 August 2010
Date of Adoption:
31 January 2010
Date of Changes:
1 August 2024
Note:
Report Reference no.
Name of Product(s) and Pharmaceutical Form(s):
Essential for inspections requested by the European Medicines Agency
Inspected Site(s):
Name and full address of the inspected site, including exact location/designation of the production facilities
Inspection Date(s):
2010-08-01
Inspector(s) and Expert(s):
Names of inspector(s), expert(s), and Competent Authority(ies)
References:
EMA reference number(s)
Inspection Findings:
Deficiencies found, with classification into critical, major, and other
Document identifier:
GMP 13
Title:
Good Measurement Practice for Ensuring Metrological Traceability
Subject:
Metrological traceability
Type of document:
Good Measurement Practice guideline
Field:
Metrology and measurement science
Issuing organization:
National Institute of Standards and Technology
Referenced standards:
International System of Units (SI)
Referenced publications:
NIST Special Publication 330; NIST Special Publication 811; ILAC P-10:2002
Scope:
Calibration and measurement traceability
Intended users:
Calibration providers and measurement laboratories
Key concepts:
Metrological traceability; calibration hierarchy; measurement uncertainty; measurement assurance
Responsibilities defined:
Calibration provider; user of measurement results
Period of application:
Not specified
Note:
Year
Year:
N/A
Region / City:
N/A
Subject:
Quality Management System Documentation
Document Type:
Standard Operating Procedure (SOP)
Organization / Institution:
N/A
Author:
N/A
Target Audience:
Employees
Period of Validity:
N/A
Approval Date:
N/A
Date of Changes:
N/A
Note:
Contextual Description
Year:
2020
Region / city:
Australia
Topic:
Pharmaceutical manufacturing, Good Manufacturing Practice (GMP)
Document type:
Guide
Organization / institution:
Therapeutic Goods Administration (TGA)
Author:
Commonwealth of Australia
Target audience:
Licensed pharmaceutical manufacturers, regulatory bodies
Effective period:
Indefinite
Approval date:
September 2020
Amendment date:
N/A
Document type:
Verification and validation protocol
Industry:
GMP-regulated manufacturing
Test type:
Installation Qualification (IQ)
Scope:
Direct impact equipment
Referenced documents:
P&ID; URS; vendor handover documentation
Acceptance criteria:
Specification conformance; correct installation; complete documentation; material certification availability
Prerequisites:
Commissioning completed; punch-list closed; trained testers
Roles involved:
Tester; validation peer reviewer; Quality Assurance
Validation activities:
Installation verification; documentation verification; peer review; QA approval
Standard:
Good Manufacturing Practice (GMP)
Year:
2026
Region / City:
Clayton, Melbourne VIC
Field:
Biotechnology, Biomedical Manufacturing
Document Type:
Job Description
Organization:
CSIRO
Author:
CSIRO
Target Audience:
Australian/New Zealand Citizens, Australian Permanent Residents, and Australian Temporary Residents with full work rights
Period of Validity:
Up to 3 years (till 30, Sept 2026)
Date of Approval:
Not specified
Date of Modifications:
Not specified
Role Overview:
This document provides detailed information on the position of GMP Technician (Downstream) at CSIRO, including job responsibilities, required competencies, and essential criteria for applicants.
Year:
2022
Theme:
Drug Registration, Good Manufacturing Practice (GMP)
Document Type:
Work Procedure
Organization / Institution:
National Medical Products Administration (NMPA), Center for Food and Drug Inspection (CFDI)
Author:
Not specified
Target Audience:
Drug regulatory authorities, manufacturing site inspection teams
Period of Validity:
Starting from January 1, 2022
Approval Date:
Not specified
Date of Changes:
Not specified
Document Type:
Application Form
Subject:
Request for Overseas Good Manufacturing Practice (GMP) Inspection
Regulatory Authority:
Health Sciences Authority
Applicable System:
PRISM
Related Guidance:
GMP Conformity Assessment of Overseas Manufacturers (GUIDE-MQA-020)
Eligible Applicants:
Singapore registered firm/company with valid Accounting and Corporate Regulatory Authority account
Required Account:
CRIS account with client code
Submitting Party:
Responsible Person or Authorised Person with Submitter or CRIS Admin role
Scope:
Overseas manufacturing sites for therapeutic products to be registered
Sections:
Company Particulars; Applicant/Authorised Person; Overseas Manufacturer Site Information; Manufacturing Operations; Responsible Persons; Outsourced Activities
Outsourced Activities Covered:
Storage; QC Testing; Manufacturing
Accreditation Reference:
ISO/IEC 17025
Receiving Unit for QSD:
Therapeutic Product Branch
Language Requirement:
English