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	<title>Courses &#8211; Global Pharma</title>
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	<link>https://globalpharmaacademy.com</link>
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	<title>Courses &#8211; Global Pharma</title>
	<link>https://globalpharmaacademy.com</link>
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	<item>
		<title>Certification course in Computer system validation</title>
		<link>https://globalpharmaacademy.com/product/certification-course-in-computer-system-validation/</link>
					<comments>https://globalpharmaacademy.com/product/certification-course-in-computer-system-validation/#respond</comments>
		
		<dc:creator><![CDATA[Admin]]></dc:creator>
		<pubDate>Wed, 08 Oct 2025 12:03:29 +0000</pubDate>
				<guid isPermaLink="false">https://globalpharmaacademy.com/?post_type=product&#038;p=4462</guid>

					<description><![CDATA[We announce Certification course in Computer system Validation

Syllabus will be as follows
TOPIC 1: basics of validation
TOPIC 2: GAMP 5
TOPIC 3: risk assessment
TOPIC 4: 21 CFR Part 11
TOPIC 5: maintenance phase
TOPIC 6: EU Annex 11

Course benefits
1)Complete domain knowledge
2)Placement assistance

Who can do
Pharma student
life science
BE ,BTech student
Frequently asked questions
1) What is computer system validation?
Ans-Validating (Testing) the software that are using in the Life science industry as GxP system and we need to ensure they are in Compliant state. We have to prepare the validation deliverables
2)What is the scope of computer system validation?
Ans-Life Science industry (Pharma +Med. Devices + Biotech) are automating and digitizing their business process. There is a huge demand for Validation Engineers.
3)Top companies providing job opportunity in computer system validation
Ans– All the Pharma companies (DRL, Novartis, Amgen, Sanofi, Takeda, Pfizer, BMS) + IT MNCs (TCS, Infosys, WIPRO, CTS, etc.)
4)How this course will help for getting opportunity in computer system validation
And– Understanding the concepts of CSV, Interpretation of the regulations and hands on experience on the validation deliverables. (Should be able to crack the interviews, understand the CSV landscape)
5)Package for CSV as fresher
And – Depends on Company starting from 2.5 LPA to 5 LPA
6)What are job roles and designation’s for CSV as fresher
Ans– CSV Analyst, Validation Engineer
7)Minimum qualification requirement for CSV
Ans – Any Degree
8)Technical skills required for CSV job
Ans – Hands on experience on Tools (ALM, JIRA, ServiceNow) is added advantage and SQL, AWS
To know more about us, kindly visit us at www.globalpharmaacadem.com or call to +91 93223 41947

Thank you]]></description>
										<content:encoded><![CDATA[<p>We announce Certification course in Computer system Validation</p>
<p>Syllabus will be as follows<br />
TOPIC 1: basics of validation<br />
TOPIC 2: GAMP 5<br />
TOPIC 3: risk assessment<br />
TOPIC 4: 21 CFR Part 11<br />
TOPIC 5: maintenance phase<br />
TOPIC 6: EU Annex 11</p>
<p>Course benefits<br />
1)Complete domain knowledge<br />
2)Placement assistance</p>
<p>Who can do<br />
Pharma student<br />
life science<br />
BE ,BTech student<br />
Frequently asked questions<br />
1) What is computer system validation?<br />
Ans-Validating (Testing) the software that are using in the Life science industry as GxP system and we need to ensure they are in Compliant state. We have to prepare the validation deliverables<br />
2)What is the scope of computer system validation?<br />
Ans-Life Science industry (Pharma +Med. Devices + Biotech) are automating and digitizing their business process. There is a huge demand for Validation Engineers.<br />
3)Top companies providing job opportunity in computer system validation<br />
Ans– All the Pharma companies (DRL, Novartis, Amgen, Sanofi, Takeda, Pfizer, BMS) + IT MNCs (TCS, Infosys, WIPRO, CTS, etc.)<br />
4)How this course will help for getting opportunity in computer system validation<br />
And– Understanding the concepts of CSV, Interpretation of the regulations and hands on experience on the validation deliverables. (Should be able to crack the interviews, understand the CSV landscape)<br />
5)Package for CSV as fresher<br />
And – Depends on Company starting from 2.5 LPA to 5 LPA<br />
6)What are job roles and designation’s for CSV as fresher<br />
Ans– CSV Analyst, Validation Engineer<br />
7)Minimum qualification requirement for CSV<br />
Ans – Any Degree<br />
8)Technical skills required for CSV job<br />
Ans – Hands on experience on Tools (ALM, JIRA, ServiceNow) is added advantage and SQL, AWS<br />
To know more about us, kindly visit us at www.globalpharmaacadem.com or call to +91 93223 41947</p>
<p>Thank you</p>
]]></content:encoded>
					
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			</item>
		<item>
		<title>Digital course on Pharmaceutical export</title>
		<link>https://globalpharmaacademy.com/product/digital-course-on-pharmaceutical-export/</link>
					<comments>https://globalpharmaacademy.com/product/digital-course-on-pharmaceutical-export/#respond</comments>
		
		<dc:creator><![CDATA[Admin]]></dc:creator>
		<pubDate>Fri, 14 Mar 2025 14:01:48 +0000</pubDate>
				<guid isPermaLink="false">https://globalpharmaacademy.com/?post_type=product&#038;p=4171</guid>

					<description><![CDATA[Following is syllabus for Digital course on pharma export

Chapter 1
Introduction to Pharma export

Chapter 2
How to export Pharmaceuticals from India

Chapter 3
How to select targeted company and location for export

Chapter 4
How to export herbals, nutraceuticals, medical devices, API from india

Chapter 5
How to find potential buyers

Chapter 6
Banking in Export

Chapter 7
How to export in USA

Chapter 8
How to export in Africa

Chapter 9
HS code, government benefits, export insurance, CHA role

Chapter 10
Case study

course benefits
-Hindi language with English subtitles
-Lifetime access
-Recorded videos
(10 modules -30 minute each)
-Free consultation after course
—Export knowledge from basics
-ISO certification of participation
-Reference book]]></description>
										<content:encoded><![CDATA[<p>Following is syllabus for Digital course on pharma export</p>
<p>Chapter 1<br />
Introduction to Pharma export</p>
<p>Chapter 2<br />
How to export Pharmaceuticals from India</p>
<p>Chapter 3<br />
How to select targeted company and location for export</p>
<p>Chapter 4<br />
How to export herbals, nutraceuticals, medical devices, API from india</p>
<p>Chapter 5<br />
How to find potential buyers</p>
<p>Chapter 6<br />
Banking in Export</p>
<p>Chapter 7<br />
How to export in USA</p>
<p>Chapter 8<br />
How to export in Africa</p>
<p>Chapter 9<br />
HS code, government benefits, export insurance, CHA role</p>
<p>Chapter 10<br />
Case study</p>
<p>course benefits<br />
-Hindi language with English subtitles<br />
-Lifetime access<br />
-Recorded videos<br />
(10 modules -30 minute each)<br />
-Free consultation after course<br />
—Export knowledge from basics<br />
-ISO certification of participation<br />
-Reference book</p>
]]></content:encoded>
					
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			</item>
		<item>
		<title>Digital course on pharma start up</title>
		<link>https://globalpharmaacademy.com/product/digital-course-on-pharma-start-up/</link>
					<comments>https://globalpharmaacademy.com/product/digital-course-on-pharma-start-up/#respond</comments>
		
		<dc:creator><![CDATA[Admin]]></dc:creator>
		<pubDate>Sat, 29 Jun 2024 09:01:15 +0000</pubDate>
				<guid isPermaLink="false">https://globalpharmaacademy.com/?post_type=product&#038;p=3772</guid>

					<description><![CDATA[Happy to announce Digital course on Pharma startup where we cover all information to start your own PCD pharma franchise or Third party manufacturing
This course is available in recorded form
Total 10 modules of 30 minutes duration each
Course Language-Hindi

Syllabus of this course is as follows

1) Basics of Pharma startup

2)Documentation and licensing

3)How to select best company and molecules

4)Team development

5)Marketing strategy

6)Managements (financial,manpower,expiry etc)

7)Channel partners]]></description>
										<content:encoded><![CDATA[<p>Happy to announce Digital course on Pharma startup where we cover all information to start your own PCD pharma franchise or Third party manufacturing<br />
This course is available in recorded form<br />
Total 10 modules of 30 minutes duration each<br />
Course Language-Hindi</p>
<p>Syllabus of this course is as follows</p>
<p>1) Basics of Pharma startup</p>
<p>2)Documentation and licensing</p>
<p>3)How to select best company and molecules</p>
<p>4)Team development</p>
<p>5)Marketing strategy</p>
<p>6)Managements (financial,manpower,expiry etc)</p>
<p>7)Channel partners</p>
]]></content:encoded>
					
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			</item>
		<item>
		<title>3 month online Certificate course in Drug regulatory Affairs</title>
		<link>https://globalpharmaacademy.com/product/certificate-course-in-drug-regulatory-affairs/</link>
					<comments>https://globalpharmaacademy.com/product/certificate-course-in-drug-regulatory-affairs/#respond</comments>
		
		<dc:creator><![CDATA[Admin]]></dc:creator>
		<pubDate>Thu, 21 Mar 2024 10:41:13 +0000</pubDate>
				<guid isPermaLink="false">https://globalpharmaacademy.com/?post_type=product&#038;p=3158</guid>

					<description><![CDATA[Syllabus
Topics covered
Class 1
i)Introduction
ii)Definition, Rationale, iii)Roles and responsibilities
Class 2
i)How Regulatory Affairs works in Pharmaceutical Company
ii)Different Regulatory Authorities
iii)Innovator and Generic Drugs
iv) Drug development process
Class 3
i)Different guidelines used in Regulatory work.
Class 4
i) ICH Guidelines
In depth Quality guidelines and Overview of Safety, Efficacy and Multidisciplinary guidelines
Class 5
CTD Structure
In depth Module wise content detailing
Class 6
i)ACTD Structure
In depth Part wise content detailing
ii) Difference between CTD and ACTD
Class 7
Dossier filing process for Europe, USA and Rest of world market
Class 8
Different types of documents required for Dossier preparation and their explanation
Class 9
Post approval process: Variations and Renewals
class 10
Overview of medical device regulatory
Class 11
Overview of Clinical Trials and their phases, Pharmacovigilance, PSUR
Class 12
Frequently asked interview questions with answers

Benefits
1)You will get certificate from ISO certified organization
2)You will get lifetime free counselling from our side
3)Recorded lectures
4)swot analysis,mock interview,skill improvement

&#160;]]></description>
										<content:encoded><![CDATA[<p>Syllabus<br />
Topics covered<br />
Class 1<br />
i)Introduction<br />
ii)Definition, Rationale, iii)Roles and responsibilities<br />
Class 2<br />
i)How Regulatory Affairs works in Pharmaceutical Company<br />
ii)Different Regulatory Authorities<br />
iii)Innovator and Generic Drugs<br />
iv) Drug development process<br />
Class 3<br />
i)Different guidelines used in Regulatory work.<br />
Class 4<br />
i) ICH Guidelines<br />
In depth Quality guidelines and Overview of Safety, Efficacy and Multidisciplinary guidelines<br />
Class 5<br />
CTD Structure<br />
In depth Module wise content detailing<br />
Class 6<br />
i)ACTD Structure<br />
In depth Part wise content detailing<br />
ii) Difference between CTD and ACTD<br />
Class 7<br />
Dossier filing process for Europe, USA and Rest of world market<br />
Class 8<br />
Different types of documents required for Dossier preparation and their explanation<br />
Class 9<br />
Post approval process: Variations and Renewals<br />
class 10<br />
Overview of medical device regulatory<br />
Class 11<br />
Overview of Clinical Trials and their phases, Pharmacovigilance, PSUR<br />
Class 12<br />
Frequently asked interview questions with answers</p>
<p>Benefits<br />
1)You will get certificate from ISO certified organization<br />
2)You will get lifetime free counselling from our side<br />
3)Recorded lectures<br />
4)swot analysis,mock interview,skill improvement</p>
<p>&nbsp;</p>
]]></content:encoded>
					
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			</item>
		<item>
		<title>3 months online Certification course in Clinical research</title>
		<link>https://globalpharmaacademy.com/product/3-months-online-certification-course-in-clinical-research/</link>
					<comments>https://globalpharmaacademy.com/product/3-months-online-certification-course-in-clinical-research/#respond</comments>
		
		<dc:creator><![CDATA[Admin]]></dc:creator>
		<pubDate>Fri, 26 Jan 2024 13:28:58 +0000</pubDate>
				<guid isPermaLink="false">https://globalpharmaacademy.com/?post_type=product&#038;p=2949</guid>

					<description><![CDATA[Syllabus
1. Introduction, History and Overview of Clinical Research
2. Drug Discovery and Development
3. Pharmacology and Toxicology
4. Who does what? / Roles and Responsibilities of various Stakeholders
5. Integrity in Clinical Research - Individual and Institutional Responsibility: Institutional review board/ Independent Ethics committee (IRB/IEC)
6. Ethics and Guidelines in Clinical Research
7. Essential documents for the conduct of a clinical trial
8. Clinical Trial Management and Budgeting
9. Regulation in Clinical Research
10. Clinical Data Management &#38; Biostatistics
11. Quality Assurance in Clinical Trials
12. Specialized Clinical Trials

Skill development classes

1) Resume preparation
2) How to search jobs
3) Expert advice
4)HR interview question discussion
5)Mock interview

Benefits
1) Certificate from ISO certified organization which is accepted worldwide
2) 100% placement assistance
3) Recorded lectures provided after live
4) Learn from 15+ year of working professionals from top MNC in india]]></description>
										<content:encoded><![CDATA[<p>Syllabus<br />
1. Introduction, History and Overview of Clinical Research<br />
2. Drug Discovery and Development<br />
3. Pharmacology and Toxicology<br />
4. Who does what? / Roles and Responsibilities of various Stakeholders<br />
5. Integrity in Clinical Research &#8211; Individual and Institutional Responsibility: Institutional review board/ Independent Ethics committee (IRB/IEC)<br />
6. Ethics and Guidelines in Clinical Research<br />
7. Essential documents for the conduct of a clinical trial<br />
8. Clinical Trial Management and Budgeting<br />
9. Regulation in Clinical Research<br />
10. Clinical Data Management &amp; Biostatistics<br />
11. Quality Assurance in Clinical Trials<br />
12. Specialized Clinical Trials</p>
<p>Skill development classes</p>
<p>1) Resume preparation<br />
2) How to search jobs<br />
3) Expert advice<br />
4)HR interview question discussion<br />
5)Mock interview</p>
<p>Benefits<br />
1) Certificate from ISO certified organization which is accepted worldwide<br />
2) 100% placement assistance<br />
3) Recorded lectures provided after live<br />
4) Learn from 15+ year of working professionals from top MNC in india</p>
]]></content:encoded>
					
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			</item>
		<item>
		<title>Online course in Pharmacovigilance</title>
		<link>https://globalpharmaacademy.com/product/online-course-in-pharmacovigilance/</link>
					<comments>https://globalpharmaacademy.com/product/online-course-in-pharmacovigilance/#respond</comments>
		
		<dc:creator><![CDATA[Admin]]></dc:creator>
		<pubDate>Sun, 14 Jan 2024 12:08:10 +0000</pubDate>
				<guid isPermaLink="false">https://globalpharmaacademy.com/?post_type=product&#038;p=2887</guid>

					<description><![CDATA[Syllabus covered
1) Overview Clinical research and History and development of PV
2) Basics of Bioequivalence, Bioavailability, Pharmacodynamics and pharmacokinetics.
3) Adverse Drug Reactions, Key Terminologies in PV, Methodologies in Pharmacovigilance
4) Clinical trials-Types, Phases
5) ICSR management and case studies
6) MedDRA coding
7) Seriousness and causality assessment
8) Narrative writing
9) Safety database overview- example- Argus, Aware, Aris g etc.
10) Special scenario in PV
11) Signal detection and management
12) Overview of Periodic Safety Update Reports (PSURs), Aggregate reporting, medical writing, Importance of local literature search
13) MICC (Medical information contact center) overview
14) Pharmacovigilance System Master File (PSMF), Risk Management Planning (RMP), Reference Safety Information (RSI)
15) PV inspection and Audits
16) Contract research organization (CRO)
17) Pharmacovigilance Regulations in Various Countries

Along with this we provide skill development classes which covers
1)zresume preparation
2)HR question
3) individual mock interview
4)Job searching skill
5)presentation skill (PPT presentation)
6)HR communication skill
7)effective email writing skill

Benefits of course
1) Certification from ISO certified organization
2) Expert guide having more than 10+ year of experience in core pharmacovigilance domain
3) Live lectures with recording
4) 100% placement assistance
5) study material provided]]></description>
										<content:encoded><![CDATA[<p>Syllabus covered<br />
1) Overview Clinical research and History and development of PV<br />
2) Basics of Bioequivalence, Bioavailability, Pharmacodynamics and pharmacokinetics.<br />
3) Adverse Drug Reactions, Key Terminologies in PV, Methodologies in Pharmacovigilance<br />
4) Clinical trials-Types, Phases<br />
5) ICSR management and case studies<br />
6) MedDRA coding<br />
7) Seriousness and causality assessment<br />
8) Narrative writing<br />
9) Safety database overview- example- Argus, Aware, Aris g etc.<br />
10) Special scenario in PV<br />
11) Signal detection and management<br />
12) Overview of Periodic Safety Update Reports (PSURs), Aggregate reporting, medical writing, Importance of local literature search<br />
13) MICC (Medical information contact center) overview<br />
14) Pharmacovigilance System Master File (PSMF), Risk Management Planning (RMP), Reference Safety Information (RSI)<br />
15) PV inspection and Audits<br />
16) Contract research organization (CRO)<br />
17) Pharmacovigilance Regulations in Various Countries</p>
<p>Along with this we provide skill development classes which covers<br />
1)zresume preparation<br />
2)HR question<br />
3) individual mock interview<br />
4)Job searching skill<br />
5)presentation skill (PPT presentation)<br />
6)HR communication skill<br />
7)effective email writing skill</p>
<p>Benefits of course<br />
1) Certification from ISO certified organization<br />
2) Expert guide having more than 10+ year of experience in core pharmacovigilance domain<br />
3) Live lectures with recording<br />
4) 100% placement assistance<br />
5) study material provided</p>
<p><span id="more-2887"></span></p>
]]></content:encoded>
					
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			</item>
		<item>
		<title>Online course in Clinical Data Management</title>
		<link>https://globalpharmaacademy.com/product/online-course-in-clinical-data-management/</link>
					<comments>https://globalpharmaacademy.com/product/online-course-in-clinical-data-management/#respond</comments>
		
		<dc:creator><![CDATA[Admin]]></dc:creator>
		<pubDate>Sun, 14 Jan 2024 11:50:07 +0000</pubDate>
				<guid isPermaLink="false">https://globalpharmaacademy.com/?post_type=product&#038;p=2885</guid>

					<description><![CDATA[Syllabus

1. Clinical Research and History

2. Clinical Drug Development

3. ICH-GCP guideline/ IEC IRB responsibilities

4. 21 CFR part 11/ Clinical trials

5. Clinical data management basic information

6. Clinical databases and types

7. Set up phase- Protocol/ CRF design/ Edit Check Specification document

8. Data Management Plan/User Acceptance Testing/ SAE document/CRF completion guideline.

9. Conduct phase- Data entry/ Medical coding/ Data cleaning

10. SAE recon/External data reconciliation/ Discrepancy management

11. Study closeout

12. Archival

&#160;

Skill development classes

&#160;

1) Resume preparation

2) How to search jobs

3) Expert advice

4)HR interview question discussion

5)Mock interview

&#160;

course Benefits

1) Certificate from ISO certified organization which is accepted worldwide

2) 100% placement assistance

3) Recorded lectures provided after live

4) Learn from top industry experts working professionals from top MNC in india]]></description>
										<content:encoded><![CDATA[<p>Syllabus</p>
<p>1. Clinical Research and History</p>
<p>2. Clinical Drug Development</p>
<p>3. ICH-GCP guideline/ IEC IRB responsibilities</p>
<p>4. 21 CFR part 11/ Clinical trials</p>
<p>5. Clinical data management basic information</p>
<p>6. Clinical databases and types</p>
<p>7. Set up phase- Protocol/ CRF design/ Edit Check Specification document</p>
<p>8. Data Management Plan/User Acceptance Testing/ SAE document/CRF completion guideline.</p>
<p>9. Conduct phase- Data entry/ Medical coding/ Data cleaning</p>
<p>10. SAE recon/External data reconciliation/ Discrepancy management</p>
<p>11. Study closeout</p>
<p>12. Archival</p>
<p>&nbsp;</p>
<p>Skill development classes</p>
<p>&nbsp;</p>
<p>1) Resume preparation</p>
<p>2) How to search jobs</p>
<p>3) Expert advice</p>
<p>4)HR interview question discussion</p>
<p>5)Mock interview</p>
<p>&nbsp;</p>
<p>course Benefits</p>
<p>1) Certificate from ISO certified organization which is accepted worldwide</p>
<p>2) 100% placement assistance</p>
<p>3) Recorded lectures provided after live</p>
<p>4) Learn from top industry experts working professionals from top MNC in india</p>
]]></content:encoded>
					
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			</item>
		<item>
		<title>Online course in Basic Medical coding</title>
		<link>https://globalpharmaacademy.com/product/online-course-in-basic-medical-coding/</link>
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		<dc:creator><![CDATA[Admin]]></dc:creator>
		<pubDate>Sat, 30 Dec 2023 07:56:50 +0000</pubDate>
				<guid isPermaLink="false">https://globalpharmaacademy.com/?post_type=product&#038;p=2882</guid>

					<description><![CDATA[&#160;

Syllabus of this course includes

1) Language of Medicine (Medical terminology, Anatomy, physiology, Pathology, Lab techniques, etc.)
2) ICD-10 CM Coding Conventions, General Coding and Chapter specific Guidelines.
3) Introduction of CPT and HCPCS coding
4) HIPAA Training (Health Insurance Portability and Accountability Act)
5) Revenue Cycle Management and Plenty of Sample coding Scenarios

&#160;]]></description>
										<content:encoded><![CDATA[<hr />
<p>Medical billing and coding is one of the fastest growing fields in the India. As industries are growing day by day according to industry data, the offshore healthcare services industry is growing at a rate of 25-35 % per year.</p>
<p>Medical coding is the fastest-growing outsourced business process in India, so trained and certified coders are required but currently very few of healthcare employers are adequately staffed with trained medical coders. The most common reason for this is the lack of qualified candidates.</p>
<p>Happy to introduce 3 months online course in Basic Medical Coding</p>
<p>This course is ideally developed for learning ICD (International classification of disease) coding</p>
<p>In this course you will get all information related to Medical coding</p>
<p>This course is available in recording format only</p>
<p>Syllabus of this course includes</p>
<p>1) Language of Medicine (Medical terminology, Anatomy, physiology, Pathology, Lab techniques, etc.)<br />
2) ICD-10 CM Coding Conventions, General Coding and Chapter specific Guidelines.<br />
3) Introduction of CPT and HCPCS coding<br />
4) HIPAA Training (Health Insurance Portability and Accountability Act)<br />
5) Revenue Cycle Management and Plenty of Sample coding Scenarios</p>
<p>In this course you also get information about Skill development which covers following information</p>
<ol>
<li>Resume preparation</li>
<li>Interview preparation</li>
<li>Email writing and job searching skills</li>
<li>Types of interview</li>
</ol>
<p>Benefits of this course</p>
<ol>
<li>You will get expert learning from top industry experts who is certified and  having 10+ year of experience</li>
<li>Skill development to become more professionals</li>
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