Training Protocol

UNIVERSITY OF CALIFORNIA, MERCED

SCIF CLEANROOM FACILITY

Cleanroom Training Protocol


Purpose

This protocol defines expectations and procedures to be followed during instrument training sessions. The goal is to ensure safe learning, proper understanding of equipment, and effective preparation for independent operation.


1. General Principles

Training is mandatory before independent instrument use.

All activities must follow cleanroom safety and contamination control protocols.

Training sessions are structured to ensure safe, repeatable, and standardized learning.

Users must actively participate and engage throughout the session.


Training Documentation and Recording

Training sessions may be recorded at the discretion of SCIF Cleanroom staff for documentation, training quality assurance, compliance, and safety purposes.

Recordings, when applicable, may be used to maintain an accurate record of training provided, support consistency and standardization of training delivery, assist in resolving discrepancies or misunderstandings regarding training content, and support compliance with facility policies and operational requirements.

Users will be informed if a training session is being recorded. Recordings will be used solely for internal facility purposes unless otherwise required by institutional policy.

By participating in the training session, users acknowledge and consent to such documentation and recording practices, when applicable.


2. Training Scope

Training is conducted using standard samples and predefined processes only.

Users are not expected to bring any materials or samples for training. The SCIF Cleanroom will provide all standard samples and required materials for training purposes.

The objective is to teach instrument operation, safety, and basic workflow.

Training does not include running or optimizing user-specific research experiments.

Users are expected to independently apply training knowledge to their own research.

General cleanroom training coverage is detailed in Section 2A.

Instrument-specific training coverage is detailed in Section 2B.


2A. General Cleanroom Training – Session Coverage

During the general cleanroom training session, the following topics and steps will be covered, including but not limited to:

Overview of cleanroom classifications (Class 100, Class 1000) and contamination control principles

Cleanroom protocols, behavior, and best practices

Gowning procedures (PPE, proper sequence, do’s and don’ts)

Entry and exit procedures (airlocks, material transfer)

Personal conduct and contamination prevention (particles, chemicals, handling)

Cleanroom safety (chemical, electrical, thermal, vacuum, and general hazards)

Equipment use policies and training requirements

Chemical handling, labeling, and storage guidelines

Waste disposal procedures (no drain disposal; use designated containers and proper labeling)

Emergency procedures (spill response, exposure, equipment failure)

Documentation and compliance (iLab usage, logging, reporting issues)

Housekeeping and maintaining a clean working environment

Communication protocols and reporting concerns

Note: Cleanroom training is mandatory prior to any facility access. Users must review all relevant manuals, SOPs, and safety materials before operating any equipment. Users are responsible for adhering to all cleanroom protocols and for conducting their own research activities independently.


2B. Instrument-Specific Training – Session Coverage

During the instrument-specific training session, the following topics and steps will be covered, including but not limited to:

Overview of the instrument purpose, capabilities, and limitations

Identification of system components, controls, and configuration

Introduction to software interface and operational controls

Step-by-step operational workflow following established SOPs

Explanation of critical process parameters and their impact on results

Instrument-specific safety considerations, hazards, and precautions

Hands-on operation under direct supervision of cleanroom staff

Proper startup and shutdown procedures

Use of standard samples and predefined processes for training purposes

Basic troubleshooting guidance within the scope of standard operation

Clean-up procedures and workspace maintenance after use

Review of common operational errors and how to avoid them

Clarification of operational boundaries and user responsibilities

Important Note: Instrument-specific training is limited to teaching safe operation, system understanding, and baseline workflow. Training does not include optimization of user-specific processes, execution of research experiments, or fabrication of devices for users. Users are responsible for independently applying training knowledge to their own research workflows.


3. Roles and Responsibilities

User Responsibility

Arrive prepared and on time for the training session

Review relevant manuals, SOPs, and instructional material beforehand

Follow all instructions provided by cleanroom staff

Actively participate and perform hands-on steps

Ask questions when clarification is needed

Maintain focus and avoid distractions during training

Follow all safety, gowning, and cleanroom protocols


Staff Responsibility

Provide structured, step-by-step instruction

Demonstrate correct operation and safety procedures

Ensure safe use of equipment during training

Answer questions and clarify operational concepts

Maintain instrument readiness and proper training environment


⚠️ Important Clarification

Cleanroom staff are not responsible for running or executing user research programs.

Staff provide training, guidance, and operational support only.

Users are fully responsible for applying training to their own experiments and research outcomes.


4. Training Workflow

A typical training session will include:

Introduction and Safety Overview

Instrument purpose and applications

Key hazards and safety precautions

System Overview

Components and controls

Software/interface introduction

Demonstration

Step-by-step operation by staff

Explanation of critical parameters

Hands-On Practice

User performs operation under supervision

Guidance provided as needed

Shutdown and Cleanup

Proper system shutdown procedure

Cleaning and workspace organization


5. Safety During Training

Follow all PPE and gowning requirements

Handle chemicals and materials only as instructed

Do not bypass safety interlocks or procedures

Immediately report any unsafe condition or incident

Stop operation if unsure about any step


6. Equipment Handling Rules

Operate controls only when instructed

Do not change parameters beyond training scope

Use only approved standard training samples

Avoid unnecessary adjustments or experimentation


7. Questions and Clarifications

Users are encouraged to ask questions at any stage

Clarification is expected before proceeding to the next step

Do not assume or guess procedures


8. Limitations of Training

Training provides foundational knowledge only

Research-specific optimization and troubleshooting are the responsibility of the user

Additional sessions may be required for proficiency


9. Training Continuation Policy

There is no limit on the number of training sessions

Users may request additional training as needed

Re-training may be required if improper usage is observed


10. Completion Criteria

Training is considered complete when the user:

Demonstrates safe operation of the instrument

Understands basic workflow and parameters

Can perform the process under supervision with minimal guidance

Staff will provide feedback regarding completion status and readiness for independent operation

Final approval for independent use is at the discretion of cleanroom staff


11. Independent Access Authorization

Independent access to instruments will be granted only after successful completion of training and fulfillment of the completion criteria.

Users must demonstrate competency and safe operation as defined in Section 10.

Cleanroom staff will evaluate performance and provide feedback regarding training completion.


Required Step (Mandatory)

Before independent access is approved:

The user must send a confirmation email to: pkumar22@ucmerced.edu

The email must include their Principal Investigator (PI)

The email must clearly state that:

The user confirms that they have successfully completed training and are competent in operating the instrument safely and correctly

There is no ambiguity regarding instrument operation

The user is ready to operate the instrument independently

⚠️ This is a required step. Independent access will not be granted without this confirmation.


Access Provisioning and Room Access (Post-Approval Process)

After receiving the required confirmation email, iLab access will be provided once the request is processed, subject to staff availability. Room access will be requested through Facilities Management (FM Help). Once the request is submitted, processing typically takes 3–5 business days. After approval, a confirmation email from FM will be shared.

Please note that while FM typically processes requests within 2–5 business days, confirmation emails may be delayed and may not be received immediately. Users are therefore advised to verify their access by visiting the cleanroom directly after the expected processing period.


12. Acknowledgment Requirement

We require that all publications, presentations, and posters acknowledge the SCIF Cleanroom Facility at UC Merced when facility resources, instruments, or expertise are utilized. Acknowledgment of facility personnel is at the discretion of the user and should follow standard academic practices.

Copies of resulting publications (PDF or link) should be provided to the facility for tracking purposes and inclusion in annual reporting.


13. Instrument and Specimen Care

When a user functions as the operator of any instrument within the SCIF Cleanroom Facility, the user assumes full responsibility for any damage to the instrument resulting from operator error, negligence, or use of inappropriate specimens. It is the operator’s responsibility to acquire sufficient training to qualify as a competent operator prior to independent use.

Specimens left in the laboratory for preparation and/or analysis will receive professional care. However, neither the facility, its employees, nor its users are responsible for accidental damage to or loss of specimens. Specimens left in the laboratory for more than 14 days may be discarded at the Principal Investigator’s (PI’s) expense unless prior arrangements are made.


14. Post-Training Expectation

Users are expected to review manuals and SOPs regularly

Apply training knowledge to their own research processes

Follow the Post-Training Troubleshooting Protocol when issues arise


15. Contact for Assistance

For any questions during or after training, please contact: pkumar22@ucmerced.edu

Cleanroom Training Protocol Acknowledgement document