All Courses
New
1
28
Training and Qualification of Personnel
Training and qualification of personnel in pharmaceutical manufacturing are essential to ensure compliance with regulatory standards, maintain product quality, and uphold Good Manufacturing Practices (GMP). A well-trained workforce minimizes errors, ensures operational efficiency, and enhances workplace safety.
W
1
28
Water System Validation SOP
User shall prepare the documents by taking into account with the relevant statutory/ in house requirements. User shall prepare documents for all the activities carried out in their department
JS
J
1
24
Java Script
welcome to java script tutorial
P
1
23
Pharma Version 003
Pharma Version 003
New
J
1
20
Java
Java
1
19
Product Quality Management
Product quality refers to how well a product satisfies customer needs, serves its purpose and meets industry standards. When evaluating product quality, businesses consider several key factors, including whether a product solves a problem, works efficiently or suits customers' purposes.
S
1
18
SOP for HPLC Operation and Maintenance
This SOP provides instructions for the routine operation, calibration, and maintenance of the High-Performance Liquid Chromatography (HPLC) system to ensure accurate and reliable analytical results.
S
1
18
SOP for Stability Studies
Stability studies are conducted to evaluate how the quality of a drug substance or drug product varies with time under the influence of environmental factors such as temperature, humidity, and light.
New
B
1
16
Biometric System(Trial)
Biometric characteristics are processed through a biometric system, which can effectively compare face, iris, fingerprint, etc. to verify or identify a person. As biometrics is on the rise, biometric systems are being integrated in the most common areas of everyday life. The most efficient one is called Automated Biometric Identification System – ABIS.
P
1
16
PHP Updated
php
New
1
15
SOP for Good Documentation Practices
Good Documentation Practices (GDP) are a set of guidelines ensuring that all pharmaceutical records are accurate, legible, traceable, and compliant with regulatory requirements. GDP is essential for m
1
15
HTML Advanced
HTML ADVANCED updated
Adhi
A
1
14
Adithya
Adithya is a student
1
12
TESTING COURSE
This is testing
New
1
12
HPLC User Maintenance & Troubleshooting
Preventative maintenance, also called PM, is the routine and regular maintenance that keeps equipment and instruments running as they should. Within this, instruments can be replaced with new or used parts, preventing downtime, and keeping your equipment working effectively and your laboratory safe.
J
1
12
JQuery
jQuery is a JavaScript Library. jQuery greatly simplifies JavaScript programming. jQuery is easy to learn.
S
1
11
SOP for Analytical Method Validation
This SOP outlines the procedure for validating analytical methods to ensure accuracy, precision, specificity, and reproducibility as per regulatory and scientific standards.
D
1
11
Document Data Control
Document Data Control
New
1
11
SOP for Stability Sample Management
Stability Sample Management ensures that pharmaceutical products are stored and tested under controlled conditions to evaluate their shelf life, potency, and quality over time. This SOP defines the procedures for handling, storing, and monitoring stability samples in compliance with regulatory guidelines such as ICH Q1A(R2).
New
I
1
10
Induction Training AD
Induction training is the process of introducing new hires to their roles and the organization
B
1
10
BSC
course
C
1
10
CA Version 004
course
GxP
G
2
10
GxP validation
LMS Course Short Introduction
New
P
1
10
Pharma Goods Storage SOP
Distribution of pharmaceutical products is an important activity in the integrated supply-chain management. Feeble points in the distribution processes of pharmaceutical products provide viable ground for counterfeit, illegally imported, stolen and substandard medicines to enter the supply chain
H
1
10
HTML
HTML
1
9
Trail version
xvzfvsd
B
1
9
BSC Version 002
course
New
D
1
9
Dry Run 07
Short Introduction
Phone model
I
1
8
I phone 13
hi this is i phone 13
B
1
8
Bio Medical version
BIO
U
1
7
User Authorization
User Authorization
weekend
1
7
The weekend - 1
The Weeknd, born Abel Makkonen Tesfaye on February 16, 1990, in Toronto, Canada, is one of the most influential and innovative music artists of the 21st century.
R
1
7
R programming
R is a programming language. R is often used for statistical computing and graphical presentation to analyze and visualize data.
M
1
7
Maths
course
New
C
3
7
Course 1
Short Introduction
H
2
7
HTML Updates
updation
R
1
7
React-JS
React-JS
S
1
6
SOP of SOP
SOP of SOP
O
1
6
OQ
oq......
E
1
6
Entry exit Procedure
The Entry and Exit Procedure is established to ensure the controlled, safe, and secure movement of personnel and visitors in and out of the facility. It supports regulatory compliance, maintains workplace discipline, and protects company assets, sensitive areas, and data.
C
1
6
CA Version 006
course
B
1
6
BA
course
E
1
6
Engineering standard version
course
J
2
6
JAVA ADVANCED
JAVA updated
F
1
5
Fresher Content
This Pharmaceutical Quality Assurance Training Certificate Program is created with the purpose of training and educating freshers
C
1
5
CA 002 Version 01
course
B
3
5
BA 003
COURSE
E
1
5
Engineering updated
Engineering
Revised
D
1
5
Disaster Management
Disaster Management Information System (DMIS) having a digital database under GIS environment is oriented towards providing information for decision makers and encompasses information on natural resources.
C
2
5
Chemistry Minor
CHEMISTRY
M
1
5
Medical version
medical
H
1
5
HTML UPDATION
HTML
s
1
4
software change & release management
This Standard Operating Procedure (SOP) details the process for managing changes made to software systems, platforms, and products owned and operated by the Archimedis Digital (AD) team. It outlines the creation, review, impact assessment, documentation, and approval of such changes, along with the procedure for releasing the modified software/product to the end-users and also describes how source code and executable repositories of software/products are controlled, maintained, and promoted through various environments. Configuration Management procedure helps in controlling changes to the configuration and maintaining the integrity and traceability of the source code and executable repositories.
Mandatory
1
4
HPLC Validation
This course focuses on the principles, methods, and practices involved in the validation of High-Performance Liquid Chromatography (HPLC) systems. HPLC is a critical technique in analytical chemistry, particularly in pharmaceuticals, biochemistry, and environmental testing. Proper validation ensures that HPLC systems deliver reliable, accurate, and reproducible results, complying with regulatory standards.
Mandatory
1
4
HPLC Validation
This course focuses on the principles, methods, and practices involved in the validation of High-Performance Liquid Chromatography (HPLC) systems. HPLC is a critical technique in analytical chemistry, particularly in pharmaceuticals, biochemistry, and environmental testing. Proper validation ensures that HPLC systems deliver reliable, accurate, and reproducible results, complying with regulatory standards.
S
1
3
SDLC - An Overview
SDLC stands for Software Development Life Cycle
S
1
3
SOP for Analytical Method Validation1
se
AM
D
1
3
Dev
Aravind Murugan is a developer
N
1
3
New SOP
dafs
A
1
3
AI Course 1
Test Data
L
1
3
LMS Revised
A learning management system (LMS) is a software application or web-based technology used to plan, implement and assess a specific learning process. In its most common form, an LMS consists of a server that performs the base functionality and a user interface (UI).
D
1
3
Dry Run 10
Short Introduction
C
1
3
CA Version 002
course
New
1
3
AD Course 01
Short Introduction
New
C
1
3
Course 002
Course 002 Short Introduction
New
F
3
3
Full Stack Developer
A full-stack developer helps build and maintain both the front-end and the back-end of a website. Learn about full-stack developer skills, salary, and how you can become one.
R
1
3
React-Updated
react
T
1
2
Training for LMS
Training for LMS
L
1
2
LMS Training
This is about the LMS module training.
em
1
2
excuse me - 1
hello
B
1
2
BA3
jj
life cycle
GxP
v
1
2
vald life cycle
The Validation Life Cycle refers to the systematic process used to ensure that a system, product, or process consistently meets predefined requirements and performs as intended. It is especially important in regulated industries like pharmaceuticals, biotechnology, and medical devices, but it's also used in software development and manufacturing.
GxP
G
1
2
GXP validation
GxP stands for “Good x Practice,” where “x” can refer to various fields such as manufacturing (GMP), clinical (GCP), and laboratory (GLP). GxP guidelines ensure that products are safe, meet quality standards, and are compliant with regulatory requirements.
S
1
2
SOP for SOP
SOP for SOP
A
1
2
AI tools
Test Data
New
1
2
eCap V14
Short Introduction
C
1
2
CA updated
course
New
1
2
Dry Run 2
Short Introduction
T
1
2
Test
ds
C
1
2
Course 002222
Course 002222
R
1
2
React
react
I
1
1
Induction Training
Induction Training
D
1
1
Deviation Management
This document describes the procedure for reporting, investigating, and managing deviations that occur during the lifecycle of software systems/products, QMS documents, and processes with in AD.
L
1
1
LMS Training 2
LMS Training 2
j
1
1
jks
ok
p
1
1
phone charger
acx
l
1
1
lap charger
xzc
color
b
1
1
blue jean
hi
levi
1
1
levis - 01
levis is a jean brand
snowflake
1
1
snowflake - 01
Snowflake is a cloud-based data platform that provides a powerful and flexible solution for data warehousing, data lakes, data engineering, data science, and data application development. Unlike traditional databases, Snowflake is built from the ground up for the cloud and supports seamless data storage, processing, and analytics at scale.
r
1
1
reqs
kj
BELO
B
1
1
Belocopia
Belo Copia is a bottle brand
LMS
T
1
1
Trail LMS
hey this course is for trail purposes.
S
1
1
SOP-QA-001rt
vgf
T
1
1
Test
Test
S
1
1
SOP-QA-004-01
sdf
S
1
1
SOP for Good Documentation Practices (GDP)9
SOP for Good Documentation Practices
New
1
1
CMMI Overview
A CMMI (Capability Maturity Model Integration) course is designed to help professionals and organizations understand and implement process improvement practices based on the CMMI framework. It provides knowledge about different maturity levels, process areas, and best practices to enhance efficiency, quality, and performance in software development, manufacturing, and service industries.
S
1
1
SOP-QA-003-01
fsgr
S
1
1
SOP-QA-002-01
Logbooks and Fomates Issuance and Control
New
L
1
1
LMS V0.1
A learning management system (LMS) is a software application or web-based technology used to plan, implement and assess a specific learning process. In its most common form, an LMS consists of a server that performs the base functionality and a user interface (UI).
B
1
1
BSC Version 01
course
P
1
1
PHARMA 03
pharma
P
1
1
Pharma 001
pharma 001
C
2
1
Chemistry
SUBJ
Mandatory
P
1
1
Personal Training
The manufacturer should have an adequate number of personnel with the necessary qualifications and practical experience. The responsibilities placed on any one individual should not be so extensive so as to present any risk to quality.
C
1
CAPA MANAGEMENT
This document describes the procedure for executing corrective and preventive actions on any non conformance (deviation) related to the product, process, and quality system discovered during design and development, sale, production, post-sale, and/or during quality audits.
U
1
User Authentication SOP
User Authentication SOP
Automation
P
1
Python Automation
Hello
name
S
1
Shri
My name is chikki
O
1
OQ 3
oq3
S
1
SOP
zxfadf
AV
A
1
Akash
Zxcsc
N
1
New SOP
x
S
1
SOP0001
HB
ac
S
1
SOP 001
This SOP outlines the procedure for planning, conducting, documenting, and evaluating GMP training for all personnel involved in GMP-regulated activities to ensure compliance with regulatory requirements and enhance employee competency.
airpods
t
1
test oq
hi hello
Coding
J
1
Jaisheeka
Python is a widely used, high-level programming language designed by Guido van Rossum and first released in 1991. Known for its simplicity, clean syntax, and ease of learning.
Coding
J
1
Jaisheeka
Python is a widely used, high-level programming language designed by Guido van Rossum and first released in 1991. Known for its simplicity, clean syntax, and ease of learning.
tester
A
1
Adithya
Jaisheeka is a dedicated and detail-oriented software tester with a strong passion for ensuring product quality and a smooth user experience.
LMS
1
LMS CONTENTS
M
validation
1
precaution
This is for validation purpose
S
1
SOP-QA-001
ok
New
1
Safe Operations on hazardous/ dangerous manufacturing processes
In manufacturing environments where hazardous materials or dangerous processes are involved, safety is paramount. Standard Operating Procedures (SOPs) are established to guide workers in performing op
NEW
A
1
AI Course 2
test data
C
1
Change Control SOP
User shall prepare the documents by taking into account with the relevant statutory/ in house requirements. User shall prepare documents for all the activities carried out in their department
New
D
1
Document Data Control Management
User shall prepare the documents by taking into account with the relevant statutory/ in house requirements. User shall prepare documents for all the activities carried out in their department
E
1
Engineering Version 0041
Engineering Version 004
New
D
2
Dry Run 14
ok
B
1
BSC Single 004
course
New
D
1
Dry Run 14
Short Introduction
New
D
2
Dry Run 13
Short Introduction
B
1
BSC Single 02
course
New
D
2
Dry Run 11
Short Introduction
C
1
CA Version 005
course
New
3
Dry Run 7
Short Introduction
C
1
CA Single 001
course
C
1
CA Standard
course
E
1
Engineering Version 004
course
N
1
Newwwwww
Tets
C
1
CSS
CSS
P
1
Pharma updated 001
Pharma 001
P
1
Pharma 004
saved
B
1
Biotechnology
Biotechnology version
H
1
HTML UPDATION 005
HTML
H
1
HTML 002
HTML
H
1
HTML VERSION
version updates
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