№ lp_2_3_41227
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This document is an inspection checklist used by the European Medicines Agency to assess Good Manufacturing Practices (GMP) compliance during EEA inspections.
Year:
2019
Region / City:
EEA
Subject:
GMP inspection
Document Type:
Inspection checklist
Organ / Institution:
European Medicines Agency (EMA)
Author:
EMA
Target Audience:
GMP inspectors
Effective Period:
Not specified
Approval Date:
19 February 2019
Date of Changes:
Not specified
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The product description is provided for reference. Actual content and formatting may differ slightly.
Year:
2026
Region:
United Kingdom
Topic:
Housing support and care services
Document type:
Survey questionnaire
Organization:
Care Inspectorate
Target audience:
Relatives or friends of service users
Key areas:
Compassion, dignity, respect, appropriate support, staffing, quality assurance, staff competence
Reference framework:
Care Inspectorate Quality Framework for Housing Support Services
Instructions:
Provide honest feedback on service quality and areas for improvement
Note:
Year
Region / city:
Great Britain
Theme:
Organic certification, import procedures
Document type:
Official form
Institution:
CERES
Author:
CERES
Target audience:
Exporters, importers, and traders in organic products
Year:
202X
Organization:
European Environment Agency (EEA)
Document type:
Guidelines / Manual
Target audience:
Policymakers, experts, general public
Format:
PDF
Content type:
Reports, executive summaries, key messages, visuals
Sections:
Key messages, executive summary, main body, annexes
Reference style:
EEA citation guidelines
Software requirements:
Microsoft Word (latest version)
Template use:
Mandatory for EEA report drafting
Year:
2026
Region / City:
European Union, European Economic Area
Theme:
Research, Data Protection, GDPR
Document Type:
Informed Consent Form
Organization / Institution:
University of California, Santa Barbara
Author:
UCSB Research Team
Target Audience:
Research Participants in the EU/EEA
Period of Validity:
Indefinite
Approval Date:
2026-02-08
Modification Date:
N/A
Issuing body:
Architects Registration Board
Route to registration:
EEA EFTA and Swiss route
Profession:
Architecture
Subject:
Professional competencies for architect registration
Document type:
Regulatory guidance and competency mapping
Applicable standards:
ARB Competency Outcomes for Architects
Competency areas covered:
Design; Research and Evaluation; Management Practice and Leadership; Professionalism and Ethics
Target audience:
Qualified EEA EFTA and Swiss architects seeking registration
Scope:
Entry to the UK Register of Architects
Key themes:
Professional competence; Practice outcomes; Environmental sustainability; Fire and life safety; Equality diversity and inclusion; Building technology
Regulatory context:
UK architectural registration requirements
Year:
2026
Region / City:
EEA, Switzerland
Topic:
Privacy Policy
Document Type:
Workplace Privacy Notice
Organization:
Viacom
Author:
Viacom Legal Team
Target Audience:
Employees, contractors, and collaborators of Viacom
Period of Validity:
Ongoing
Approval Date:
2026-02-17
Amendment Date:
N/A
Note:
Year
Topic:
Immigration, Visa Application
Document Type:
Application Form
Organization / Institution:
Gibraltar Immigration Department
Target Audience:
EEA Residents seeking entry into Gibraltar
Year:
2023
Region / City:
European Union
Subject:
Customs Union, Legislative Proposal
Document Type:
Legislative Proposal
Organization / Institution:
European Parliament, European Commission, European Union
Author:
European Commission
Target Audience:
EU policymakers, national governments, customs authorities, legal experts
Period of Validity:
Ongoing
Approval Date:
N/A
Date of Amendments:
N/A
Note:
Year
Subject:
CO2 emissions, fuel consumption, heavy-duty vehicles, electric vehicles
Document type:
Regulation
Issuing body:
European Commission
Target audience:
Member States, national authorities, economic operators
Year:
2014-2021
Programme:
EEA Grants
Project number:
EHP-CZ-MOP-1-xxx
Academic year:
20../20..
Participant:
Student of Higher Education Institution
Sending institution:
Name, Faculty/Department, Country
Receiving institution:
Name, Faculty/Department, Country
Traineeship title:
As specified in Table A
Planned mobility period:
from [DD/MM/YY] to [DD/MM/YY]
Learning outcomes:
Knowledge, skills, and competences expected by the end of the traineeship
ECTS credits awarded:
yes/no, specify number if applicable
Insurance:
Accident and liability coverage provided by sending and/or receiving institution
Commitment:
Approved by student, sending institution, and receiving institution
Year:
2021
Region / City:
Ireland
Topic:
Financial Services / Investment Firms
Document Type:
Notification Form
Authority:
Central Bank of Ireland
Author:
Not specified
Target Audience:
Investment Firms, Regulatory Authorities
Effective Period:
36 months
Approval Date:
Not specified
Amendment Date:
Not specified
Context:
A notification document for investment firms wishing to establish or modify a branch in another EEA state under MiFID II regulations.
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:
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
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