Improving Laboratory Performance through Method Validation & Method Verification Batch VI, Bandung 23 – 24 September 2010

Untuk mengetahui performance suatu metode secara periodik seiring dengan perubahan kinerja peralatan laboratorium yang digunakan di dalam metode uji tersebut, dan untuk memenuhi persyaratan ISO 17025 yang salah satu klausulnya mensyaratkan validasi metode uji sehingga presisi dan akurasinya bisa dipertanggung jawabkan.

GARIS BESAR MATERI TRAINING TATA CARA VALIDASI / METHOD VALIDATION

1. General Overview
2. Method Validation against Method Verification
3. Testing Method & Measurement Process
4. Investigating Measuremet Sensitivity (Detection Limit and Quantitation Limit)
5. Establishing Linearity of Measurement
6. Estimation of Highest Limit of Measurements
7. Determination of Accuracy and Precision
8. Comparison to Reference Method
9. Investigating Method Selecctivity
10. Determination of Method Ruggedness/Robustness

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Implementing an Effective Health and Safety Program in the Laboratory Batch VIII, Bandung 29 – 30 September 2010

There are many categories of hazards that might be encountered in a laboratory setting, and situations can change frequently. Even after you have identified and controlled all current risks, it is critical that you remain open to the possibility that new unexpected dangers can arise. Periodically verify the hazards are required. All employees who work with hazardous chemicals must be apprised of the hazards of chemicals present in their work area. This training must be provided before initial assignment and before new exposure situations. Personal protective equipment necessary for the safe handling of hazardous substances must also be provided. Employees who work with chemicals in laboratories must be trained on the Laboratory Standard. Additional training is required when new exposure situations arise. Such situations include the use of new chemicals, greater quantities of chemicals, and different procedures.

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Enhancing Laboratory Performance by Internal Quality Control Program Batch VI, Bandung 28 – 29 Oktober 2010

Globalization drags all business sectors into a very tight competition, resulting in the improvement of  quality  of products and services. Only the ones that have a competent laboratory applying a good and systematic quality control process can survive against this competition. We are eager to share experiences by helping industries, organization, government institution, laboratory and other business sectors understand and implement activities in maintaining the competence & quality of their testing laboratory

OBJECTIVE
After having been trained, all trainees are expected to be able to make sure that the data produced by the laboratory through a systematic process of quality control  are reliable and eliminate any possible mistakes and minimize every error in the process of analysis

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Four Days Comprehensive Training on Estimation of Measurement Uncertainty, Bali 23 – 26 November 2010

Uncertainty in measurement, now becomes a crucial parameter for laboratory testing or calibration results. So many training provided out there introducing laboratory people to the concept of the UNCERTAINTY, many of the trainees say the training gives  the UNCERTAIN output.  We learnt from the experiences and we will not give you the UNCERTAINTY but we will give the CERTAIN TRAINING of the ESTIMATION MEASUREMENT UNCERTAINTY. Besides, many industrial sectors strictly applied the uncertainty parameter as their requirement. So, for the labs want to achieve the capability of providing uncertainty of measurement, our training program is the right answer.

OBJECTIVE
After having been trained,  all the trainees are expected to absorb the essence of the philosophy of the training material and be able to calculate the estimation of uncertainty and apply it in the result of analysis or calibration and have a deep knowledge of how to overcome the difficulties in estimating the uncertainty.

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GLP (Good Laboratory Practices) Batch IX, Bandung 29 – 30 September 2010

MANFAAT TRAINING GLP

1. Memahami persyaratan “Principles of Good Laboratory Practices”
2. Memahami interpretasi persyaratan “Principles of Good Laboratory Practices”
3. Memahami prinsip-prinsip penyiapan laboratorium yang memenuhi “Principles of Good Laboratory Practices”

MATERI TRAINING GLP

1. Sejarah GLP
2. GLP vs ISO 17025
3. Prinsip GLP menurut OECD : Pengenalan Umum, Poin-Poin Dasar GLP
4. Sumber Daya : Personalia, Fasilitas
5. Aturan : Protokol atau Rencana Studi (Penelitian), SOP
6. Karakterisasi : Item Uji, Sistem Uji
7. Dokumentasi : Data Mentah & Pengumpulan Data, Laporan Akhir, Arsip, Pemberian Indeks
8. Unit Penjaminan Mutu : Audit Laporan Akhir dan Data mentah, Pernyataan Penjaminan Mutu, Inspeksi Suplier dan Kontraktor , Pengedaran dan Pengarsipan Laporan dan Arsip Unit Penjaminan Mutu

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