sop for Accident Management Procedures

 

sop for Accident Management Procedures

 

1.0 Objective
To lay down a procedure for providing immediate medical attention /care to the injured employee in

case of accident within factory and ensure arrangement of suitable medical assistance.
2.0 Scope
This standard operating procedure is applicable for all employees posted at abc company.
3.0 Responsibility
3.1 All Supervisor of HR & Administration
3.2 Manager/ Head Concern Area
4.0 Abbreviations and Definitions
SOP : Standard Operating Procedure
HRD : Human Resource Department
CC NO : Change Control Number
cGMP : Current Good Manufacturing Practice
HOD : Head of Department
ESI scheme : The health insurance scheme administered by a corporation
constituted under the provisions of Employees State
Insurance Act, 1948
5.0 Procedure
5.1 After accident has been reported from the concerned department, functionary from Human Resource Development

department shall reach on the spot at once and enquire into the matter. He/ she shall make available First Aid

to the injured person(s) immediately.
5.2 The details of accident shall be provided to the Factory Manager or his/her designee immediately

by HRD department and appropriate advice shall be obtained.
5.3 In case of serious injury, the injured persons(s) shall be taken to the concerned ESI dispensary/hospital,

if such person is covered under the ESI Scheme. Otherwise, the injured person(s) shall be taken to the nearest

hospital by ambulance or available transportation mode.
5.4 Head, HRD/ designee along with one person shall accompany the injured person to the hospital.
5.5 The near and dear ones of the injured person may be informed at the address furnished in the records of the

company about the accident, if situation allows.
5.6 A comprehensive Accident Report (Annexure-I) shall immediately be prepared and forwarded by the concerned Executive/Officer/Supervisor/Incharge on duty to the HRD department through departmental head for necessary

information, appropriate action and records.
5.7 Head, HRD/ designee shall incorporate conclusions and suggestions to the Accident Report and put up

to Factory Manager for suitable consideration.
5.8 Head, HRD/ designee shall record the accident in Form No. 27 as required under the Provisions

of Factories Act, 1948, and ESI Act, 1948 respectively.
6.0 Forms and Records
6.1 Accident Report – Annexure-1
7.0 Distribution
7.1 Master Copy – Documentation Cell (Quality Assurance)
7.2 Controlled Copy – Quality Assurance, Personnel & Administration.
8.0 History

Revision Number Details For Change
Reason for Revision
00 New SOP NA
process validation protocol for methylcobalamin niacinamide and pyridoxine injection

validation protocol of sterility test

sop for Analytical Method Transfer

Protocol for hold time study of sterile garments

sop for process validation

sop for swab sampling for validation of clean surfaces

cleaning validation maco and noel calculation formula

sop for performance qualification for analyst

Sop for Validation report for disinfectant efficacy

Sop for Method validation report for bacterial endotoxin test

Sop for method validation microbiology sterility testing

sop for validation report for preservative efficacy test

sop for Protocol cum report for efficacy qualification of uv light

sop for validation protocol for uv light efficacy of dpb & laf

sop for cleaning validation protocol tablet manufacturing equipment



sop for cleaning validation protocol ointment manufacturing equipment

concurrent process validation for rabeprazole ec and domperidone sr capsules

sop for Validation for cleaning procedure liquid injection

sop for Validation for cleaning procedure dry powder injection

sop for validation plan

Preparation Approval Control and Distribution of Master Formula Records

calibration policy for equipment and instruments

sop for stability management

evaluation Sampling of Raw Materials questionnaire

training evaluation questionnaire

sop for approval of Contract Parties

sop for Operation and Cleaning of Purified Water Generation System

sop for Storage of Standard Weights

process validation protocol for methylcobalamin niacinamide and pyridoxine injection

validation protocol of sterility test

sop for Analytical Method Transfer

Protocol for hold time study of sterile garments

sop for process validation

sop for swab sampling for validation of clean surfaces

cleaning validation maco and noel calculation formula

sop for performance qualification for analyst

Sop for Validation report for disinfectant efficacy

Sop for Method validation report for bacterial endotoxin test

Sop for method validation microbiology sterility testing

sop for validation report for preservative efficacy test

sop for Protocol cum report for efficacy qualification of uv light

sop for validation protocol for uv light efficacy of dpb & laf

sop for cleaning validation protocol tablet manufacturing equipment



sop for cleaning validation protocol ointment manufacturing equipment

concurrent process validation for rabeprazole ec and domperidone sr capsules

sop for Validation for cleaning procedure liquid injection

sop for Validation for cleaning procedure dry powder injection

sop for validation plan

Preparation Approval Control and Distribution of Master Formula Records

calibration policy for equipment and instruments

sop for stability management

evaluation Sampling of Raw Materials questionnaire

training evaluation questionnaire

sop for approval of Contract Parties

sop for Operation and Cleaning of Purified Water Generation System

sop for Storage of Standard Weights

sop for Verification of Weighing Balance

sop for Receipt of Returned Goods from Market

Preparation of Master Formula Record MFR

  sop for Leave Policy

     Sop for Submitting of Leave Application

 sop for Accident Management Procedures

 

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