A Laboratory Information Management System (LIMS) is a software solution used in laboratories to manage large amounts of sample data and laboratory workflow. It typically handles five key phases: sample receipt and login, assignment and tracking, processing and quality control, data storage, and result reporting. A LIMS provides advantages like faster access to reports, reduced errors, improved efficiency and productivity. However, it also requires training, time for adaptation, costs for purchase and maintenance, and backup systems in case of data loss. Laboratories must ensure proper management, security and validation of any LIMS.
Laboratory information management system (LIMS)JYOTIRMOY ROY
A Laboratory Information Management System (LIMS) is software that allows you to effectively manage samples and associated data to improve lab efficiency. By using a LIMS, your lab can automate workflows, integrate instruments, and manage samples and associated information.
Purpose of a LIMS is to improve lab efficiency and accuracy by reducing manual operations. A LIMS system will perform a range of core functions. These include - Workflow management,
Record keeping, Inventory management, Reporting.
There will be differences between various LIMS systems, such as mobile-access, customization options and the level of technical support provided.
Introduction of Automation of the Analytical Process
Unit Operations
Specimen identification
Specimen preparation
Specimen delivery
Specimen loading and aspiration
Specimen processing
Sample induction and internal transport
Reagent handling and storage
Chemical reaction phase
Measurement approaches
Signal processing, data handling and process control
Applications of automation in clinical lab
Use of laboratory instruments and specimen processing equipment to perform clinical laboratory assays with only minimal involvement of technologist .
Automation in clinical laboratory is a process by which analytical instruments perform many tests with the least involvement of an analyst.
The International Union of Pure and Applied Chemistry (IUPAC) define automation as "The replacement of human manipulative effort and facilities in the performance of a given process by mechanical and instrumental devices that are regulated by feedback of information so that an apparatus is self-monitoring or self adjusting”.
Laboratory information management system (LIMS)JYOTIRMOY ROY
A Laboratory Information Management System (LIMS) is software that allows you to effectively manage samples and associated data to improve lab efficiency. By using a LIMS, your lab can automate workflows, integrate instruments, and manage samples and associated information.
Purpose of a LIMS is to improve lab efficiency and accuracy by reducing manual operations. A LIMS system will perform a range of core functions. These include - Workflow management,
Record keeping, Inventory management, Reporting.
There will be differences between various LIMS systems, such as mobile-access, customization options and the level of technical support provided.
Introduction of Automation of the Analytical Process
Unit Operations
Specimen identification
Specimen preparation
Specimen delivery
Specimen loading and aspiration
Specimen processing
Sample induction and internal transport
Reagent handling and storage
Chemical reaction phase
Measurement approaches
Signal processing, data handling and process control
Applications of automation in clinical lab
Use of laboratory instruments and specimen processing equipment to perform clinical laboratory assays with only minimal involvement of technologist .
Automation in clinical laboratory is a process by which analytical instruments perform many tests with the least involvement of an analyst.
The International Union of Pure and Applied Chemistry (IUPAC) define automation as "The replacement of human manipulative effort and facilities in the performance of a given process by mechanical and instrumental devices that are regulated by feedback of information so that an apparatus is self-monitoring or self adjusting”.
Laboratory Information Management System (LIMS) is one of the systems which is effective in different areas, whether they be industrial or medical etc.,
The PPT explain about the NABL and accreditation process according to the ISO 17025. And how you will get benefited with the NABL/ISO 17025 accreditation for your Lab.
Quality control (QC) is a procedure or set of procedures intended to ensure that a manufactured product or performed service adheres to a defined set of quality criteria or meets the requirements of the client or customer. QC is similar to, but not identical with, quality assurance (QA).
QC IN clinical biochemistry labs and hospitals
This slide will give you brief idea about different types of laboratory control records used in pharmaceutical industries & where it is used.
I hope this will help you a bit .
For any corrections, do not hesitate to comment down below.
How medical/clinical laboratory staff should behave. Their relationship with their regulatory body, their clients, their colleagues and other professionals.
Phụ lục 11 về Hệ thống máy tính trong bộ tiêu chuẩn GMP EU. Xem thêm các tài liệu khác trên kênh Slideshare của Công ty cổ phần Tư vấn thiết kế GMP EU.
Laboratory Information Management System (LIMS) is one of the systems which is effective in different areas, whether they be industrial or medical etc.,
The PPT explain about the NABL and accreditation process according to the ISO 17025. And how you will get benefited with the NABL/ISO 17025 accreditation for your Lab.
Quality control (QC) is a procedure or set of procedures intended to ensure that a manufactured product or performed service adheres to a defined set of quality criteria or meets the requirements of the client or customer. QC is similar to, but not identical with, quality assurance (QA).
QC IN clinical biochemistry labs and hospitals
This slide will give you brief idea about different types of laboratory control records used in pharmaceutical industries & where it is used.
I hope this will help you a bit .
For any corrections, do not hesitate to comment down below.
How medical/clinical laboratory staff should behave. Their relationship with their regulatory body, their clients, their colleagues and other professionals.
Phụ lục 11 về Hệ thống máy tính trong bộ tiêu chuẩn GMP EU. Xem thêm các tài liệu khác trên kênh Slideshare của Công ty cổ phần Tư vấn thiết kế GMP EU.
Why should you invest in a Lab Information Management SystemPragadeesh Suresh
A Lab Management Software is simply a tool that can ease the operations involved in modern laboratories by automating most of them. As an all-inclusive software including lab management system, ERP tools, data analytics tool and virtual software, LIMS efficiently works out on the laboratory informatics.
Why should you invest in a Lab Information Management System?MocDoc
A Lab Management Software is simply a tool that can ease the operations involved in modern laboratories by automating most of them. As an all-inclusive software including lab management system, ERP tools, data analytics tool and virtual software, LIMS efficiently works out on the laboratory informatics. While each of the operations involved in LIMS is possible manually, why should one choose the software? Here is why:
https://mocdoc.in/blog/why-should-you-invest-in-a-lab-information-management-system
Qualis LIMS has built-in integrated modules to manage all laboratory processes and can be deployed with minimal to no customisation required.
Our LIMS software fits laboratories across multiple industries namely Pharmaceuticals, Lifesciences, Cell and Gene Therapy, Biopharmaceutical, Healthcare, Diagnostics, Life-sciences, Oil & Gas, Chemicals, Agricultural , Clinical Research, Contract Research Organisation, Biobank, Dairy, Drug Discovery
The lab management module in a hospital is a vital component of a comprehensive healthcare management system, often considered the best healthcare management system. This system, sometimes referred to as a smart hospital management system, is an integrated software solution designed to streamline and optimize various aspects of healthcare administration and patient care. The lab management module plays a crucial role in this ecosystem.
Việc duy trì kiểm soát các điều kiện môi trường trong các phòng thí nghiệm hoặc phòng sạch được quản lý chặt chẽ để tuân thủ các tiêu chuẩn GMP. Tuy nhiên việc này phức tạp và tốn thời gian. Hướng dẫn này đưa ra một số khía cạnh quan trọng cần xem xét để giảm thiểu rủi ro và duy trì sự tuân thủ trong phòng thí nghiệm hoặc phòng sạch.
Xem thêm các tài liệu khác trên kênh của Công ty Cổ phần Tư vấn Thiết kế GMP EU.
6.COMPUTERS AS DATA ANALYSIS.pptxB.Pharm sem 2 Computer Applications in PharmacyVedika Narvekar
Computers as data analysis in Preclinical development:
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Defecation
Normal defecation begins with movement in the left colon, moving stool toward the anus. When stool reaches the rectum, the distention causes relaxation of the internal sphincter and an awareness of the need to defecate. At the time of defecation, the external sphincter relaxes, and abdominal muscles contract, increasing intrarectal pressure and forcing the stool out
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Normal defecation is painless, resulting in passage of soft, formed stool
CONSTIPATION
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IMPACTION
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DIARRHEA
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FLATULENCE
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FECAL INCONTINENCE
Fecal incontinence is the inability to control passage of feces and gas from the anus. Incontinence harms a patient’s body image
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ACCORDING TO apic.org,
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ACCORDING TO pewtrusts.org,
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VISION
Being proactive
Supporting optimal animal and human health
Exploring ways to reduce overall use of antimicrobials
Using the drugs that prevent and treat disease by killing microscopic organisms in a responsible way
GOAL
to prevent the generation and spread of antimicrobial resistance (AMR). Doing so will preserve the effectiveness of these drugs in animals and humans for years to come.
being to preserve human and animal health and the effectiveness of antimicrobial medications.
to implement a multidisciplinary approach in assembling a stewardship team to include an infectious disease physician, a clinical pharmacist with infectious diseases training, infection preventionist, and a close collaboration with the staff in the clinical microbiology laboratory
to prevent antimicrobial overuse, misuse and abuse.
to minimize the developme
2. Laboratory Information Management System (LIMS) is a
software-based solution that is used in labs for data
management and to process a large number of lab samples to
manage laboratory workflow.
3.
4.
5.
6.
7.
8.
9. Functionalities of LIMS
Usually divided into five laboratory processing phase:
1. the reception and log in of a sample and associated customer data,
2. the assignment, scheduling, and tracking of the sample and the
associated analytical workload,
3. the processing and quality control associated with the sample and
the utilized equipment and inventory,
4. the storage of data associated with the sample analysis,
5. the inspection, approval, and compilation of the sample data for
reporting and/or further analysis
10. Functionalities of LIMS (Additional)
1. Audit management
2. Barcode handling
3. chain of custody
4. Compliance
5. Customer relationship
management
6. document management
7. instrument calibration and
8. maintenance
9. inventory and equipment
management
10. manual and electronic data
entry
11. method management
12. personnel and workload
management
13. quality assurance and
control
14. Reports
15. time tracking
16. Traceability
17. workflows
12. 1. Very fast report access & queries
2. Reduction in paperwork
3. Improved data quality (reduction in errors)
4. Improved operational efficiency
5. Simple to use Excel-like formulas
6. Increased productivity (reduction of routine tasks)
7. Productivity gains (instrument interfacing and auto-reporting)
8. Integration with other departments/business systems
9. Reduces transcription errors
10. Increases throughput
11. Avoids duplication
12. ROI (Return On Investment is typically within 1 year)
Advantages of LIMS
14. Disadvantages of LIMS
1. Training—Personnel training is required
2. Time to adapt to a new system
3. Cost—Purchase and maintenance are the most expensive parts
of a computerized system, and the costs can be prohibitive in
some settings.
4. Physical restrictions
5. Need for back-up system—All computer information must be
carefully backed up.
6. Loss of data due to a damaged disk or system crash cannot be
tolerated, and backup systems will be critical
15.
16. 5.10 Laboratory information management
Previously included as Annex B (informative) – now has become a requirement
17. 5.10.1 General
The laboratory shall have access to the data and information needed to provide a service
which meets the needs and requirements of the user.
The laboratory shall have a documented procedure to ensure that the confidentiality of
patient information is maintained at all times.
NOTE In this International Standard, “information systems” includes the management of
data and information contained in both computer and non-computerized systems. Some
of the requirements may be more applicable to computer systems than to non-
computerized systems. Computerized systems can include those integral to the functioning
of laboratory equipment and stand alone systems using generic software, such as word
processing, spreadsheet and database applications that generate, collate, report and
archive patient information and reports.
18. 5.10.2 Authorities and responsibilities
• The laboratory shall ensure that the authorities and responsibilities for
the management of the information system are defined, including the
maintenance and modification to the information system(s) that may
affect patient care.
•The laboratory shall define the authorities and responsibilities of all
personnel who use the system, in particular those who:
a) access patient data and information;
b) enter patient data and examination results;
c) change patient data or examination results;
d) authorize the release of examination results and reports
19. 5.10.3 Information system management
The system(s) used for the collection, processing, recording,
reporting, storage or retrieval of examination data and
information shall be:
a) validated by the supplier and verified for functioning by the
laboratory before introduction, with any changes to the system
authorized, documented and verified before implementation;
NOTE Validation and verification include, where applicable, the
proper functioning of interfaces between the laboratory
information system and other systems such as with laboratory
instrumentation, hospital patient administration systems and
systems in primary care.
20. 5.10.3 Information system management
b) documented, and the documentation, including that for day to day functioning of
the system, readily available to authorized users;
c) protected from unauthorized access;
d) safeguarded against tampering or loss;
e) operated in an environment that complies with supplier specifications or, in the
case of non-computerized systems, provides conditions which safeguard the
accuracy of manual recording and transcription;
f) maintained in a manner that ensures the integrity of the data and information
and includes the recording of system failures and the appropriate immediate and
corrective actions;
g) in compliance with national or international requirements regarding data
protection.
21. 5.10.3 Information system management
• The laboratory shall verify that the results of examinations,
associated information and comments are accurately reproduced,
electronically and in hard copy where relevant, by the information systems
external to the laboratory intended to directly receive the information (e.g.
computer systems, fax machines, e-mail, website, personal web devices).
When a new examination or automated comments are implemented, the
laboratory shall verify that the changes are accurately reproduced by the
information systems external to the laboratory intended to directly receive
information from the laboratory.
22. 5.10.3 Information system management
• The laboratory shall have documented contingency plans to
maintain services in the event of failure or downtime in information systems
that affects the laboratory’s ability to provide service.
• When the information system(s) are managed and maintained off-
site or subcontracted to an alternative provider, laboratory management
shall be responsible for ensuring that the provider or operator of the system
complies with all applicable requirements of this International Standard.
23.
24.
25. CONCLUSION
1. A computerized system for laboratory data is often called a laboratory
information management system and is referred to by the acronym LIMS
or LIS.
2. The use of a computerized system is becoming more common in
laboratories around the world.
3. An appropriately designed and installed LIMS brings accuracy and
accessibility to the flow of samples and data in the clinical laboratory.
26.
27. KEY Messages
A good Laboratory Information Management System will:
• Will ensure all data - the final product of the laboratory - is well
managed
• Ensure confidentiality and privacy of patient information
• Incorporate all the laboratory business processes as a part of the
system
• Assure the accessibility, accuracy, timeliness and security of data
• Streamline sample tracking and sample workflow in the clinical
laboratory