Root Cause Analysis (RCA) For Corrective And Preventative Action (CAPA)

Root Cause Analysis (RCA) For Corrective And Preventative Action (CAPA) – The primary objective of this course is to develop an understanding of the principles and techniques involved in the practice of RCA (Root Cause Analysis).  Emphasis is placed on the practical aspects of how to perform an analysis.  In addition, this course will provide effective methods which can be used with a Corrective Action system to helps you and your team to ensure costly issues are resolved quickly and do not get dropped through the cracks. The course will provide the attendees with a system to categorize all types of issues, assign responsibility and track team activities to resolve important issues. Attendees will also learn advanced skills in root cause analysis, problem prevention, and continuous improvement.  Included will be the identification of the characteristics and changes that have contributed to simple and complex problems, and how to fix them, as well as, working with the tools and templates to capture all needed data to comply with CAPA  (Corrective and Preventative Action) reports.

 

MATERI:

  1. Efficient root cause analysis programs
  2. Developing effective training programs to ensure compliance
  3. Respond effectively to non-conformances, failures, deviations and complaints by identifying root causes and implementing corrective and preventative actions
  4. Developing and implementing programs to prevent reoccurrence
  5. Essential SOPs and Other Documentation
  6. Understand and interpret OOS results
  7. Increase accuracy through efficient documentation practices
  8. Areas of FDA concerns
  9. Identify and track deviations and non-conformances
  10. Respond to complaints and deviations with corrective and preventative actions
  11. Analyze and trend data to identify existing and potential causes of non-conformance
  12. Integrate RCA with other systems: internal auditing, CAPA and complaint handling
  13. Gather, organize and manage the data required to conduct RCA
  14. Determine whether or not a complaint should go through a CAPA program
  15. Determine internal and external reporting requirements
  16. Write effective SOPs
  17. Verify and validate a CAPA program
  18. Perform trend analysis and use effective RCA tools (Flow Charting, Fault Tree Analysis, Fishbone Diagrams, etc.)
  19. Optimize CAPA and RCA documentation procedures
  20. Analyze FDA Warning Letters and common citations to avoid non-compliance

 

INSTRUKTUR:

Ratna Hindria D P S, SE, MSi, Ak, CA and Tim

 

METODE:

Kegiatan pelatihan dirancang agar peserta dapat memahami secara komprehensif materi yang disampaikan, sehingga dapat dimplementasikan secara aplikatif dalam dunia kerja. Adapun metode yang digunakan adalah:

  1. Presentation
  2. Discuss
  3. Case Study
  4. Evaluation

 

PESERTA:

This course is intended for all personnel concerned with quality and the analysis & correction of problems.  The material will be presented in such a way as to be of value to varying levels of expertise among the participants, and will be pragmatic in emphasis.  It will be particularly valuable to those newer to this field or those who wish to refresh their knowledge of these technologies.

 

FASILITAS:

  1. Training Hand Out
  2. Digital Material
  3. Certificate
  4. Exclusive Souvenir
  5. Qualified Bag
  6. Training Photo
  7. Training room with full AC facilities and multimedia
  8. Once lunch and twice coffee break every day of training
  9. Qualified Instructor

 

Jadwal Pelatihan 2024

JAN - FEBMAR - APRMEI - JUNJUL - AGSTSEP - OKTNOV - DES
2 - 4 Jan5 - 7 Mar1 - 3 Mei2 - 4 Jul5 - 7 Sept5 - 6 Nov
9 - 11 Jan12 - 14Mar7 - 9 Mei9 - 11 Jul12 - 14 Sept12 - 13 Nov
17 - 19 Jan19 - 21 Mar14 - 16 Mei16 - 18 Jul19 - 21 Sept19 - 20 Nov
23 - 25 Jan26 - 28 Mar
21 - 23 Mei23 - 25 Jul27 - 28 Sept26 - 27 Nov
30 Jan - 1 Feb2 - 4 Apr28 - 30 Mei30 Jul - 1 Agst3 - 5 Okt3 - 4 Des
6 - 8 Feb16 - 18 Apr4 - 6 Jun6 - 8 Agst10 - 12 Okt10 - 11 Des
13 - 15 Feb23 - 25 Apr11 - 13 Jun13 - 15 Agst15 - 16 Okt17 - 18 Des
20 - 22 Feb18 - 20 Jun27 - 29 Agst24 - 26 Okt23 - 24 Des
27 - 29 Feb25 - 27 Jun29 - 31 Agst29 - 30 Okt

Waktu dan tempat:

Pukul 08.30 – 16.00 WIB

Hotel Berbintang di Yogyakarta

Request for Training Venue: Semarang, Solo, Bandung, Jakarta, Balikpapan, Surabaya, Jogja, Lombok, Malang, Makassar and Batam

In House Training Depend on request

 


FORMULIR PENDAFTARAN TRAINING (FORM PRA REGISTRASI)

INFORMATION OPTIONS

Judul Training (wajib)

Tanggal Pelatihan

Jenis Registrasi (wajib)


PERSONAL DATA

Nama Anda (wajib)

Perusahaan

Jabatan

Alamat Perusahaan

Email (wajib)

Telepon Seluler/No. Hp (wajib)

Telepon Kantor

No. Ekstensi

Facsimile/Fax

Website


PRE REGISTRATION DATA (TIDAK MENGIKAT)

Penanggung Jawab Training di Perusahaan

Email Perusahaan

Office Phone + Ext atau No. Handphone

Jumlah Peserta

Nama-nama Peserta

Pembayaran

Pesan untuk Penyelenggara Training

 

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