DR MANISH-2.pdf laser proctology piles and fistula

Jan 27, 20250 likes19 views

Get the best piles and fistula treatment in Jaipur with advanced laser proctology techniques. Dr. Manish Rajput, a renowned specialist, provides painless, quick, and highly effective treatments for piles, fissures, and fistula. Using cutting-edge laser technology, the procedures ensure minimal discomfort, no stitches, and faster recovery, helping patients return to their daily lives with ease. Dr. Rajput is committed to offering personalized care and long-term solutions, ensuring lasting relief and improved quality of life. With his expertise and modern facilities, you can expect safe and reliable treatment for all proctological conditions.

D R M A N I S H
RAJPUT
ht t ps://dr manishr ajput .com
Bookan appointment!

IN T R O D U C T IO N
Dr
. Manish Rajput is an I
nterventional
Radiologist & Team Lead, Team I
R
Jaipur
. They are the biggest team of
I
nterventional Radiologists. They are
trained from Tata Memorial Center
,
Mumbai, I
ndia. They have worked in so
many government and corporate
hospitals across the country.

Medical school (MBBS):2005-2011: -People’s
Medical College, Bhopal(MP)
DNB (Radio diagnosis):
- Apollo hospital,
Hyderabad(Telangana)
FVIR (PDCC):- Tata Memorial Centre,
Mumbai(Maharashtra)
Senior Resident: Hinduja Hospital Mumbai, SMS
Hospital Jaipur
Past Visiting Doctor:Leelavati Hospital Mumbai,
Breach Candy Hospital Mumbai, Wockhardt
Hospital Mumbai, Hinduja Hospital Mumbai
Ex Assitant Professor:JNU Medical College, Jaipur
Currently Working as Senior Consultant
Interventional Radiologist in various corporate
hospitals of Rajasthan based in Jaipur
HIS
EDUCATION

S T R E N G T H S
Ilead the biggest I
R team in the state.
Vast portfolio for I
R services.
All the team members are from Tata
Memorial Hospital, Mumbai.
Extensive experience in performing and
interpreting basic Radio-Diagnosis.
Gained experience in performing
I
nterventional Radiologic procedures.
Ipossess oratory skill by speaking at
numerous industry events.
Ability to teach complex concepts in a basic
manner
.

Varicose Veins Prostate Artery Embolization PRG
Biopsy and
fNAC
Angioplasty & Venoplasty PCN & DJ Stenting
O
U
R
S
E
R
V
I
C
E
S

+91 7729021111
dr.manish@infinityintervention.com
O-5-A, Adinath Marg, Near Surya
Hospital, C Scheme, Ashok Nagar,
Jaipur, Rajasthan 302001
C ON TA C T
US!

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Good Automated Laboratory Practices (GALP) Standards, Compliance, and Impleme...Dr. Smita Kumbhar

36 slides•263 views

Good Automated Laboratory Practices (GALP) refers to a structured framework designed to ensure the reliability, accuracy, and integrity of data generated by automated laboratory systems. These practices encompass standard operating procedures (SOPs), regulatory compliance, software validation, and personnel training to maintain consistency in laboratory operations. GALP is essential for laboratories that rely on automation to process high volumes of data while ensuring regulatory adherence, particularly in pharmaceutical, biotechnology, and clinical research environments. Principles of GALP The fundamental principles of GALP include: 1. Data Integrity: Ensuring accurate, reliable, and tamper-proof data recording and analysis. 2. Regulatory Compliance: Adhering to national and international standards such as ISO, 21 CFR Part 11, and QCI guidelines. 3. Standardized Processes: Implementing well-defined SOPs to guide laboratory operations. 4. System Validation: Regularly verifying automated instruments and software for functionality and compliance. 5. Personnel Training: Ensuring that laboratory staff are adequately trained to operate automated systems efficiently and accurately. 6. Risk Management: Identifying and mitigating potential risks in automated workflows. 7. Continuous Improvement: Periodic reviews and updates to laboratory practices to incorporate technological advancements. GALP Requirements To implement GALP, laboratories must adhere to certain requirements: 1. Standardized Documentation: Maintaining comprehensive records of laboratory procedures and automation processes. 2. Software and Instrument Validation: Ensuring that all automated systems function as intended and comply with regulatory requirements. 3. Data Security Measures: Implementing encryption, access control, and audit trails for secure data management. 4. Regulatory Compliance: Aligning with relevant regulations such as 21 CFR Part 11, ISO standards, and QCI guidelines. 5. Personnel Competency: Conducting periodic training and assessments for laboratory staff. 6. Audit Readiness: Preparing for internal and external inspections by maintaining up-to-date documentation. SOPs of GALP Standard Operating Procedures (SOPs) form the backbone of GALP. These SOPs cover: 1. Instrument Calibration: Regular calibration and validation of automated instruments. 2. Data Entry and Management: Guidelines on recording, storing, and retrieving data in compliance with regulatory standards. 3. Sample Handling: Ensuring standardized procedures for sample collection, processing, and storage. 4. Software Usage and Maintenance: Guidelines on software validation, updates, and troubleshooting. 5. Audit Trail Management: Recording and reviewing all modifications made to electronic data. 6. Corrective and Preventive Actions (CAPA): Addressing non-compliance and implementing necessary improvements. Training Documentation A key aspect of GALP is personnel training, which includes: 1. Training Plans

Detailed Overview of the Drugs and Cosmetics Act, 1940 & RulesDr.Navaneethakrishnan S

23 slides•242 views

This presentation provides a comprehensive overview of the Drugs and Cosmetics Act, 1940, and its associated rules from 1945. It covers the objectives of the Act, its significance in regulating the import, manufacture, distribution, and sale of drugs and cosmetics in India. Key definitions such as drugs, cosmetics, misbranded, adulterated, and spurious products are explained in detail. Additionally, it highlights the legal definitions and important schedules to the Act, ensuring clarity on regulatory standards. Essential roles such as Drug Inspector and Government Analyst are also discussed. This presentation is useful for pharmacy students, regulatory professionals, and individuals interested in pharmaceutical law.

Let's Talk About It: Ovarian Cancer (Making Meaning after a Cancer Diagnosis)RheannaRandazzo

19 slides•313 views

Making meaning from hardship is a complex conversation. Many cancer survivors feel the delicate balance between making meaning and the internalized or external pressure that often follows a cancer diagnosis. Questions such as “What now?” are common when treatment ends. Well-meaning friends and family may subtly (or not so subtly) expect us to behave or view the world differently. If figuring out who you are now feels puzzling, join us on Wednesday, December 11th. Together, we will discuss how changes in your identity and perspective are a valid and essential part of this journey. Research has shown us how making meaning after hardship facilitates adjustment and well-being.

urine formation.pptx kidney urine formationPooja Rani

27 slides•126 views

Time-Limited Innovation for CLL Control: Changing the Treatment Story With Ev...PVI, PeerView Institute for Medical Education

40 slides•18 views

Chair, Nitin Jain, MD, discusses chronic lymphocytic leukemia in this CME/AAPA activity titled “Time-Limited Innovation for CLL Control: Changing the Treatment Story With Evidence and Emerging Consensus on 1L BTKi -BCL2i Combinations.” For the full presentation, downloadable Practice Aid, and complete CME/AAPA information, and to apply for credit, please visit us at https://bit.ly/4gi5jVw. CME/AAPA credit will be available until April 3, 2026.