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      <image:title>CDSCO Adds European Union to Rule 63's Recognised Jurisdictions, Tightens Class A NSNM Self-Certification</image:title>
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      <image:title>CDSCO Introduces Ninth Schedule Testing Fees and Mandatory Sterilization Site Labeling</image:title>
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      <image:title>CDSCO Extends Pediatric Warning to All Chlorpheniramine and Phenylephrine FDCs</image:title>
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      <image:title>Schedule H1 Set to Add Flupentixol, Zopiclone, Gabapentin and Carisoprodol: What G.S.R. 745(E) Proposes</image:title>
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      <image:title>CDSCO Flags Enclomiphene as an Unapproved New Drug — Manufacturing and Marketing Under Scanner</image:title>
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      <image:title>CDSCO Directs IND Division to Process Import Permission for New Drugs Backed by Ongoing Phase III Global Clinical Trials</image:title>
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      <image:title>Drugs (Twelfth Amendment) Rules, 2026: CDSCO Widens Form 29 Licence Categories Under Rule 89</image:title>
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      <image:title>India introduces formal debarment for false or fabricated documents in drug licensing</image:title>
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      <image:title>CDSCO’s Revised Guidance on Common Submission Format for Import &amp; Registration of Drugs: What Changed in 2026</image:title>
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      <image:title>DPCO (Amendment) Order, 2026: Overcharging Liability Relief for Pharma manufacturers</image:title>
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      <image:title>CDSCO Directs Ibuprofen Manufacturers to Add 'Fixed Drug Eruption' to Prescribing Information Leaflets</image:title>
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      <image:title>No Registration Certificate, No Entry for Imported Cosmetics</image:title>
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      <image:title>CDSCO Clarifies Jurisdiction for Compounding of Offences Applications</image:title>
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      <image:title>CDSCO Notifies Final Guidance Document on Medical Device Software (MDSW)</image:title>
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      <image:title>When a “+” Sign Isn’t Just a Plus</image:title>
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      <image:title>DCC intends to tighten control on manufacturing and supply of printed packaging materials used for drugs</image:title>
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      <image:title>High-Alcohol Oral Formulations Move Into Schedule H1</image:title>
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    <loc>https://vaayath.com/blog/183</loc>
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      <image:title>DCC Recommends Mandatory Public Disclosure of Suspended and Cancelled Drug Licenses</image:title>
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      <image:title>D&amp;C Amended to Cover Licensing of Stem Cell Products, Gene Therapeutics and Xenografts</image:title>
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      <image:title>Schedule H2 Expanded: Antimicrobials and Many Other Drugs Now Under Stricter Controls</image:title>
    </image:image>
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      <image:title>CDSCO Restricts IVF Supplies to Registered ART Centres</image:title>
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      <image:title>CDSCO Issues Clarity on New Drugs, DC Granules &amp; MR Pellets Licensing</image:title>
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      <image:title>Centre Bans 16 Fixed Dose Combinations Under Section 26A of Drugs &amp; Cosmetics Act</image:title>
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      <image:title>India Cracks Down on Chloramphenicol &amp; Nitrofurans in Food Producing Animals</image:title>
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      <image:title>CDSCO Directs All Drug Manufacturers to Establish Pharmacovigilance Systems Under Schedule M</image:title>
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      <image:title>India brings Pregabalin under Schedule H1</image:title>
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      <image:title>CDSCO Issues Stern Warning Against Injectable Cosmetics and Misleading Beauty Claims</image:title>
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      <image:title>CDSCO Orders Nationwide Crackdown on Unauthorised GLP-1 Weight Loss Drugs</image:title>
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      <image:title>Drug Applications with Unanswered Queries to Be Rejected Within 30 Days by CDSCO</image:title>
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      <image:title>⚖️ “No Approval, No Market”: Delhi High Court Sends a Strong Message on Unapproved Drugs &amp; FDCs</image:title>
    </image:image>
  </url>
  <url>
    <loc>https://vaayath.com/blog/86</loc>
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      <image:title>India Bans High-Dose Nimesulide: What You Need to Know</image:title>
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      <image:title>Compounding of Offences under the Drugs and Cosmetics Act, 1940: What Stakeholders Need to Know</image:title>
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      <image:title>CDSCO Directive on Immediate Inspections as per Revised Schedule M – Is Your Facility Ready?</image:title>
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      <image:title>🚨 Bringing in the effect of GST change on Drugs &amp; Medical Devices - A challenge made easy</image:title>
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      <image:title>CDSCO Issues Regulatory Clarification on Combi-Pack Approvals: Key Insights for Injectable Manufacturers</image:title>
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      <image:title>🚨 Regulatory Update: Major Amendments to the Cosmetics Rules, 2020: Advancing Clarity, Compliance, and Consumer Protection</image:title>
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      <image:title>🛡️ The Role of Pharmacovigilance in Post-Marketing Surveillance: The Silent Guardian of Patient Safety</image:title>
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      <image:title>Quality Audit: A Critical Tool for Continuous Improvement in Quality Systems</image:title>
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      <image:title>📢 WHO-GMP COPP Application via ONDLS Portal: CDSCO New Mandate from July 2025</image:title>
    </image:image>
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      <image:title>💊 Understanding Adverse Drug Reactions (ADRs)/ Adverse Drug Events (ADEs)- Every Pharma Company Should Know</image:title>
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      <image:title>🚨 New Drug Licenses Need CDSCO Approval: DCC Reinforces Regulatory Compliance</image:title>
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    <loc>https://vaayath.com/blog/98</loc>
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      <image:title>🚨 CDSCO Issues Urgent Directive for Stopping manufacturing and marketed of Unapproved FDCs – What Pharma Manufacturers Need to Know</image:title>
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      <image:title>📊 Unlocking Opportunity: Comprehensive Market Research Reports Now Available at Vaayath Consulting</image:title>
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      <image:title>🌐Ease of Doing Business: CDSCO introduces new Updates regarding the Auto-generated Market standard Certificate (MSC) and Non-Conviction Certificate (NCC) for Licenced Medical devices.</image:title>
    </image:image>
  </url>
  <url>
    <loc>https://vaayath.com/blog/101</loc>
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      <image:title>Government Mandates Online CRO Registration via SUGAM Portal!</image:title>
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      <image:title>NPPA Directs Drug Price Cuts Following Customs Duty Exemptions</image:title>
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      <image:title>CDSCO Issues Urgent Directive for Category D FDC Manufacturers: Submit Applications by May 24, 2025</image:title>
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      <image:title>Navigating Regulatory Changes: Gastro-Resistant &amp; Delayed-Release Drugs as ‘New’ Under NDCT Rules 2019</image:title>
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      <image:title>Government Orders Immediate Withdrawal of manufacturing and export permissions of Tapentadol Carisoprodol Combinations</image:title>
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      <image:title>CDSCO Introduces Online Process for Additional Variant Applications in Cosmetics</image:title>
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      <image:title>India Imposes National Ban on Nimesulide for Veterinary Use Due to Toxicity Risks</image:title>
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      <image:title>Major Relief for MSME Pharma Manufacturers: MoHFW Extends Deadline for Revised GMP Compliance</image:title>
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      <image:title>Pharmacovigilance system compliance in India</image:title>
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      <image:title>Simplifying Clinical Trial Amendment Approvals in India</image:title>
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      <image:title>Navigating Drug Rules in India: A Guide for Pharmaceutical Marketers</image:title>
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      <image:title>CDSCO Issues Directive to Expedite Approvals for Rare Disease Medications</image:title>
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      <image:title>Best API Registration of Drugs in India</image:title>
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      <image:title>What are CDSCO Form MD 26 and 27 and the benefits of having the import license for new medical devices?</image:title>
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      <image:title>How To Get Wholesale Drug License in India?</image:title>
    </image:image>
  </url>
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      <image:title>Safe Handling of Narcotic and Psychotropic Drugs in a Wholesale Warehouse: A Complete Guide</image:title>
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      <image:title>Solubility of Active Pharmaceutical Ingredients</image:title>
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      <image:title>Labelling Provisions of Drugs in India</image:title>
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      <image:title>Test License for Import of Drugs in India</image:title>
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      <image:title>Test License for Manufacturing New Drug in India</image:title>
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      <image:title>Overview of Drug Registration Process for Import in India</image:title>
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    <lastmod>2024-05-16</lastmod>
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      <image:title>New Drugs Approval Services</image:title>
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      <image:title>CDSCO launches NSWS portal for medical device licensure</image:title>
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      <image:title>USFDA approves TARPEYO to reduce the loss of kidney function in adults with primary IgAN</image:title>
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      <image:title>EU publishes its first list of critical medicines to avoid potential shortages</image:title>
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      <image:title>US Firm Issues Nationwide Recall of Himalayan Pain Relief Tea Due to the Presence of Hidden Drug Ingredients, Diclofenac and Dexamethasone</image:title>
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      <image:title>India introduces new set of standards for GMP of Pharmaceutical Products</image:title>
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      <image:title>CDSCO waives off requirement of TSE BSE certification</image:title>
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      <image:title>CDSCO issues draft notification for Schedule H2 drugs</image:title>
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      <image:title>Test License for drugs in India</image:title>
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      <image:title>Nuances of conducting interview during audit</image:title>
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      <image:title>CDSCO extends timeline for FDC regularization</image:title>
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      <image:title>CDSCO granted restricted EUA to vaccinate children</image:title>
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      <image:title>Communication during Audit</image:title>
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      <image:title>CDSCO publishes updated list of banned drugs in India</image:title>
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      <image:title>Online Drug Licensing process in India – Portal Registration</image:title>
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      <image:title>Conflict Management among Audit team during Audit</image:title>
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      <image:title>Conflict Management during audit</image:title>
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      <image:title>Time Management during Audit</image:title>
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      <image:title>Auditor - Blend of knowledge and skills</image:title>
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      <image:title>ISO 22301: Maintaining Business Continuity</image:title>
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      <image:title>Types of Glass used for Pharmaceutical Packaging</image:title>
    </image:image>
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      <image:title>Britain has become the first country to approve Lagevrio (Molnupiravir)</image:title>
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      <image:title>Ethics Committee Regulations in India</image:title>
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      <image:title>Mutual Recognition Agreement</image:title>
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      <image:title>Reference Standard for testing pharmaceuticals</image:title>
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      <image:title>Pathway for regularization of FDCs declared as rational</image:title>
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      <image:title>Impurities in Pharmaceutical preparation</image:title>
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      <image:title>USFDA approved the first fully licensed COVID19 vaccine</image:title>
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      <image:title>Audit - An Integral Part of Organization Success</image:title>
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      <image:title>Friability Testing of Granules and Spheroids</image:title>
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      <image:title>Friability Testing of Tablets</image:title>
    </image:image>
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    <lastmod>2021-04-06</lastmod>
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      <image:title>Data Integrity and Principles of ALCOA and ALCOA+</image:title>
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      <image:title>New Drug Approval Process in India</image:title>
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      <image:title>Chronicles of FDC Ban in India</image:title>
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      <image:title>Periodic or Skip Testing</image:title>
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      <image:title>Parametric Release</image:title>
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    <loc>https://vaayath.com/blog/168</loc>
    <lastmod>2020-11-25</lastmod>
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      <image:title>Pharmaceutical Specifications</image:title>
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    <lastmod>2020-11-12</lastmod>
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      <image:title>Site Master File – The Gateway to Manufacturing Site</image:title>
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    <lastmod>2020-10-31</lastmod>
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      <image:title>Product Quality Review</image:title>
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