№ lp_1_12917
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This document is a sample biosafety manual for laboratory use, outlining procedures, protocols, and risk assessments for handling biological and rDNA materials.
Year:
Not specified
Region / City:
Not specified
Subject:
Laboratory biosafety
Document Type:
Manual
Organization / Institution:
Not specified
Author:
Not specified
Target Audience:
Laboratory personnel, safety officers
Period of Validity:
Not specified
Approval Date:
Not specified
Date of Changes:
Not specified
Price: 8 / 10 USD
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The product description is provided for reference. Actual content and formatting may differ slightly.
Year:
2021
Region / city:
Weymouth, Dorset
Subject:
Microbiological monitoring of shellfish contamination
Document type:
Protocol
Institution:
Cefas
Author:
L. Coates
Target audience:
Harvesters, collectors, local authorities
Effective period:
N/A
Approval date:
17/11/2021
Amendment date:
N/A
Document Type:
Laboratory sample submission form
Purpose:
Registration and testing of samples
Testing Scope:
Microbiological analysis
Requested Tests:
Total Aerobic Microbial Count; Total Yeast and Mould Count; Bile-Tolerant Gram Negative Bacteria; Presence of S. aureus; Presence of Pseudomonas spp.; Presence of P. aeruginosa; Presence of E. coli; Presence of Coliforms; Presence of Salmonella; Presence of C. albicans; Presence of C. sporogenes; Other specified tests
Fields Included:
Company Name; Purchase Order; Quotation Number; Mailing Address; Submitted by; Contact Details; Sample Description; Batch Number; Quantity or Number of Items; Specifications; Special Requirements
Administrative Notes:
RUSH service conditions; OOS exception investigation; Validation requirement; SSF submission and amendment policy
Intended Users:
Clients submitting samples for laboratory testing
Year:
2026
Region / City:
Nesher, Israel
Subject:
Microbiological and chemical analysis of cosmetics and water
Document Type:
Laboratory report
Organization:
Institute for Food Microbiology and Consumer Goods Ltd.
Author:
Laboratory staff
Target audience:
Regulatory bodies, manufacturers, and quality assurance personnel
Testing scope:
Cosmetic products, drinking water, mineral water, recreational water, wastewater
Standards referenced:
USP, Ph. Eur., JP, ISO, SM, SI
Test methods:
Microbial identification, antimicrobial effectiveness, microbial enumeration, physicochemical measurements
Sample types:
Cosmetic products, soil, aggregates, drinking water, mineral water, recreational water, wastewater
Date of issue:
2026
Endorsing standards:
U.S. Pharmacopeia, European Pharmacopoeia, Japanese Pharmacopeia, Israeli Standards, ISO
Note:
Year
Theme:
Microbiological diagnostics, Rickettsial infections, Chlamydia, Mycoplasma
Document type:
Educational material
Target audience:
Students, medical professionals
Contextual description:
A medical educational document focusing on the microbiological diagnostics of infections caused by rickettsia, chlamydia, and mycoplasma, detailing the properties, transmission, pathogenesis, clinical findings, and laboratory diagnosis of these infections.
Year:
Not specified
Location:
St Georges Hospital, Blackshaw Road, Tooting, SW17 0QT
Department:
Renal Unit, Courtyard Clinic
Subject:
Microbiological and chemical testing of dialysis water
Document Type:
Service specification
Testing Frequency:
Weekly
Sample Location:
Renal Unit Courtyard Clinic, Ring Road, St Georges Hospital
Parameters Tested:
TVC, Endotoxin, Copper, Fluoride, Magnesium, Nitrates, Potassium, Sodium, Aluminium, Calcium, Arsenic, Cadmium, Chromium, Lead, Sulphate, Barium, Silver, Thallium, Zinc, Chlorine, Mercury, Beryllium
Action Levels:
TVC > 50 CFU/mL and > 100 CFU/mL; Endotoxin > 0.12 EU/mL and > 0.25 EU/mL
Reporting Requirements:
Sampling and testing dates, measured values with units, interpretation against ISO 23500-4:2024 and Renal Association recommendations, notification of exceedances
Turnaround Time:
Two days to two weeks depending on test type
Quality Control Measures:
Certified reference materials, equipment calibration, external quality assessment, documented procedures
Applicable Standard:
ISO 23500-4:2024 Preparation and quality management of fluids for haemodialysis and related therapies
Review Period:
Annual review with written amendments by mutual agreement
Year:
2020
Region / City:
Hampton, VA
Subject:
Microbiological and Nutritional Analysis Testing
Document Type:
Combined Synopsis/Solicitation
Agency:
Department of Veterans Affairs
Author:
Warren A Pennil
Target Audience:
Registered businesses in SAM
Period of Validity:
January 13, 2020 - November 30, 2024
Date of Approval:
January 9, 2020
Date of Changes:
N/A
Year:
2023
Region / City:
Andhra Pradesh, India
Theme:
Surgical site infections, abdominal surgeries, microbiology, risk factors
Document Type:
Research study
Author:
Dr. Syamala
Target Audience:
Medical professionals, researchers in surgery and infectious diseases
Study Period:
January 2023 - December 2024 (estimated)
Date of Approval:
Not specified
Date of Changes:
Not specified
Year:
2023
Region / city:
Global
Topic:
Microbial Control, Sterilization Techniques, Disinfection
Document Type:
Educational Material
Organization / Institution:
Not specified
Author:
Not specified
Target Audience:
Students, Researchers in Microbiology, Laboratory Technicians
Period of Validity:
Ongoing
Approval Date:
Not specified
Date of Modifications:
Not specified
Year:
2023
Region:
United Kingdom
Subject:
Microbiological contamination, antimicrobial resistance
Document type:
Research report
Institution:
UK Health Security Agency
Author:
Frieda Jorgensen
Target audience:
Veterinary public health professionals, researchers
Sample type:
Raw dog and cat food
Parameters measured:
Pack weight, cost, E. coli counts, presence of Salmonella spp.
Methodology:
Retail survey and microbiological analysis
Findings:
Pack weight moderately associated with Salmonella detection, no significant association with E. coli counts or cost
Year:
2026
Organization:
Department of Agriculture, Fisheries and Forestry (DAFF)
Document type:
Policy / Procedure Manual
Version:
7.3
Scope:
Biosecurity industry participants
Audit types:
Probationary Audit Rate, Low Audit Rate
Compliance categories:
Critical non-compliance, Major non-compliance, Minor non-compliance
Key arrangement outcomes:
Containment, Isolation, Security, Identification, Traceability, Hygiene, Movement, Release, Awareness, Inspection, Treatment, Arrangement compliance, Notification, Supporting functions
Target audience:
Biosecurity industry participants
Fee structure:
On site $62/15min, Off site $37/15min
Reference conditions:
Biosecurity containment level 2 (BC2), Microbiological Class 5.2
Documented procedures:
Audit checklist, Site mapping, Signage, Access control, Waste storage
Year:
2020
Region / City:
USA
Topic:
Biosafety, Laboratory Systems, Public Health
Document Type:
Email Communication
Organization / Institution:
Centers for Disease Control and Prevention (CDC)
Author:
Division of Laboratory Systems, CDC
Target Audience:
Laboratory professionals, clinicians, and leadership in rural and community hospitals
Period of Action:
Not specified
Approval Date:
Not specified
Date of Modifications:
Not specified
Year:
2025
Institution:
Click here to enter text
Reporting period:
1 January 2025 – 31 December 2025
Submission deadline:
1 March 2026
Document type:
Annual report
Responsible body:
Institutional Biosafety Committee (IBC)
Contact:
Department of Biosafety, [email protected]
Activities covered:
LMO/rDNA projects, modifications to approved projects, exempted activities, LMO storage, incidents and occupational disease records
Approval requirements:
Verification by IBC Chair, signed Declaration page
Format:
Soft copy with formal cover letter
Note:
Year
Document type:
Reporting format
Legal framework:
Cartagena Protocol on Biosafety; Nagoya – Kuala Lumpur Supplementary Protocol on Liability and Redress
Responsible organization:
Executive Secretary of the Convention on Biological Diversity
Target audience:
National focal points and relevant stakeholders
Period covered:
From [month/year] to [month/year]
Submission date:
[day/month/year]
Languages:
One of the six official United Nations languages
Instructions:
Online and offline submission options available
Mandatory questions:
Yes
Content focus:
National measures, biosafety integration, pharmaceuticals regulation, stakeholder consultation
Year:
2024
Note:
Region / City
Subject:
Institutional Biosafety
Document Type:
Self-Assessment Tool
Organ / Institution:
National Institutes of Health (NIH)
Author:
NIH Office of Science Policy (OSP)
Target Audience:
Institutional Biosafety Committees, Research Institutions
Year:
2018
Region / City:
Ithaca, New York
Topic:
Biological Safety
Document Type:
Risk Assessment
Institution:
Cornell University
Author:
Cornell University Environmental Health and Safety (EHS)
Target Audience:
Laboratory personnel, biosafety officers
Period of Effectiveness:
Ongoing
Approval Date:
January 2018
Amendment Date:
Not specified
Year:
2020
Region / City:
United States
Subject:
Biosafety, Laboratory Systems
Document Type:
Email Communication
Organization:
Centers for Disease Control and Prevention (CDC)
Author:
Division of Laboratory Systems, CDC
Target Audience:
Laboratory professionals, clinicians, leadership in rural and community hospital settings
Period of Validity:
Ongoing
Approval Date:
Not specified
Modification Date:
Not specified
Year:
2025
Note:
Region / City
Topic:
Biosafety
Document Type:
Manual
Institution / Organization:
National Institutes of Health (NIH), NAU Institutional Biosafety Committee (IBC)
Target Audience:
Laboratory Personnel, Principal Investigators (PIs)
Year:
2024
Note:
Region / City
Topic:
Biosafety
Document Type:
Report
Year:
2007
Region / City:
Putrajaya
Topic:
Biosafety
Document Type:
Form
Organization / Institution:
Department of Biosafety
Author:
N/A
Target Audience:
Institutions registered with the National Biosafety Board
Period of Validity:
N/A
Approval Date:
N/A
Date of Amendments:
N/A
Year:
2020
Region / City:
Putrajaya
Topic:
Occupational health, biosafety
Document Type:
Form
Organ / Institution:
National Biosafety Board
Author:
Not specified
Target Audience:
Laboratory personnel, Principal Investigator
Validity Period:
Not specified
Approval Date:
Not specified
Date of Changes:
Not specified
Contextual Description:
Occupational disease/exposure investigation form used for reporting occupational exposure to LMO/rDNA materials in biosafety settings.