Looking to sell or distribute medical devices in India? The MD‑42 License is a must-have for legal compliance, credibility, and access to e-commerce platforms. This license, issued under the Medical Devices Rules, 2017, applies to retailers, wholesalers, and importers. Learn how to apply, required documents, fees, and more in this simple, step-by-step guide. 👉 https://www.psrcompliance.com/blog/md-42-license-in-india
BIS Certification for home appliances is a mandatory compliance requirement in India that ensures products meet safety, quality, and performance standards set by the Bureau of Indian Standards. It safeguards consumers from substandard products and helps manufacturers build trust, gain market acceptance, and avoid legal issues. The certification process involves application submission, product testing in BIS-recognized labs, and factory inspections. With BIS certification, home appliance manufacturers and importers can enhance brand credibility and expand market reach. Learn the complete process, benefits, and requirements in our detailed guide here: https://www.psrcompliance.com/blog/bis-certification-for-home-appliances
WPC Certification is an official approval required for importing, manufacturing, or selling wireless devices in India such as Bluetooth speakers, drones, Wi-Fi routers, and walkie-talkies. Issued by the Wireless Planning & Coordination (WPC) Wing under the Department of Telecommunications, it ensures that devices operate within permitted frequency ranges and meet safety standards. This certification helps prevent interference with other wireless services, ensures smooth customs clearance, and builds market credibility. Businesses must obtain WPC ETA before launching wireless-enabled products in India to stay compliant and avoid legal issues. Learn more: https://www.psrcompliance.com/wpc-certification
Starting a business in India in 2025? Learn the complete step-by-step process for company registration, including DSC, DIN, SPICe+ filing, name approval, and post-incorporation compliance. This guide will help you navigate the legal requirements with ease and set up your business quickly and correctly. Read more: https://www.psrcompliance.com/blog/company-registration-steps-2025
EPR Registration for e-waste is essential for producers, importers, and brand owners of electronic products in India. This guide covers everything you need to know in 2025 – from eligibility and document requirements to the step-by-step registration process, fees, and post-registration compliance.
Looking to start a pharmacy, wholesale drug business, or manufacturing unit in Haryana? This blog covers everything you need to know about obtaining a drug license in Haryana — including types of licenses, eligibility, required documents, application process, validity, and how to avoid rejection. Whether you're applying for a retail, wholesale, or manufacturing drug license, this complete guide will help you stay compliant with the Drugs and Cosmetics Act, 1940. PSR Compliance offers expert assistance in drug license registration and a range of other compliance services like EPR registration, PSARA license, BIS certification, APEDA registration, NGO registration, and more. 👉 Read the full guide at: https://www.psrcompliance.com/blog/drug-license-in-haryana
Securing a drug license, such as Form 20B for wholesale or Form 20 for retail under India’s Drugs and Cosmetics Act, 1940, is a critical step for pharmacists and distributors. However, applicants often face significant delays, sparking debates about whether the system is inherently broken or merely sluggish due to bureaucratic inefficiencies. Governed by the Central Drugs Standard Control Organization (CDSCO) and State Drugs Standard Control Organizations (SDSCOs), the licensing process is designed to ensure drug safety and compliance but frequently frustrates stakeholders with prolonged timelines. This article explores the causes of delays, evaluates the system’s functionality, and offers strategies to navigate it effectively.
Manufacturing medical devices in India—especially Class C and Class D devices—requires proper regulatory approval from the Central Drugs Standard Control Organization (CDSCO). One such crucial approval is the MD-42 license, issued under the Medical Device Rules, 2017. This guide explains everything manufacturers need to know about the MD-42 license in India, including its purpose, process, documents required, and how to stay compliant with Indian medical device regulations.
Obtaining an MD-42 license is a critical step for manufacturers looking to legally produce Class C and D medical devices in India. With increasing global demand, stringent compliance standards, and growing market opportunities, having the right license not only ensures legal safety but also boosts your credibility in the healthcare ecosystem.
EPR Registration for E-Waste is mandatory for producers, importers, and brand owners under India’s E-Waste Management Rules. To comply, you must register with CPCB, submit required documents (GST, IEC, product details), obtain your EPR Authorization Certificate, meet annual collection targets, and file regular returns. This ensures your business manages e-waste responsibly while avoiding penalties. EPR compliance not only protects the environment but also builds a sustainable brand image. Learn more here: https://www.psrcompliance.com/blog/epr-registration-for-e-waste-in-india-2025
An MD-42 License is an official authorization issued to medical device distributors or sellers in India. It permits the sale, stocking, exhibition, and distribution of notified medical devices classified under various categories as per Indian regulations. Without this license, dealing in such medical devices is illegal and can attract penalties or prosecution.
In a country like India, where a significant portion of the population is under the age of 15, the toy market is both vast and influential. With that comes the responsibility of ensuring that toys are safe, reliable, and non-toxic for children of all age groups. Unsafe toys pose serious risks—choking hazards, sharp edges, harmful chemicals, and electrical malfunctions. That's why the Indian government, through the Bureau of Indian Standards (BIS), has made toy safety a national priority.
CSR-1 is a mandatory electronic form introduced by the Ministry of Corporate Affairs (MCA). It is the first step NGOs must complete to be eligible to receive CSR funding under Section 135 of the Companies Act, 2013.
✅ What is a Drug License? A drug license is a legal permit issued by the State Drug Control Authority or CDSCO, depending on the nature of the business. It ensures that the handling, sale, and distribution of drugs and medicines are done in a safe, regulated, and authorized manner. 📍 Types of Drug Licenses in Haryana There are several types of licenses you can apply for, depending on your business activity: Retail Drug License (RDL): For pharmacies and chemist shops selling to end consumers. Wholesale Drug License (WDL): For businesses selling medicines to retailers or hospitals. Manufacturing Drug License: For units involved in drug or cosmetic manufacturing. Loan License: For firms without manufacturing facilities, using another manufacturer’s site. Import License: For importing drugs or cosmetics from outside India. 📋 Documents Required for Drug License in Haryana Here are the key documents you’ll need: Application form (as per the license type) Covering letter with purpose and business details Proof of business premises (rental deed or ownership) Site layout plan and key plan Electricity bill or NOC for premises Affidavit of full-time registered pharmacist or qualified technical staff Registration certificate of pharmacist (in case of retail license) Qualification & experience certificates (for wholesale license) Identity & address proof of partners/directors Partnership deed or company registration certificate Photo of premises and storage facility (refrigerator, etc.) GST registration (if applicable) Challan of fee payment via Haryana drug portal 📝 How to Apply for a Drug License in Haryana (Online) Here’s a simplified step-by-step process: Visit the official Haryana Drug Control Portal Go to: https://xenya.haryana.gov.in/ Register your business Create your login credentials and choose the type of license. Fill the application form online Upload the required documents and details. Pay the government fee online Use the portal’s payment gateway to pay as per your license category. Schedule an inspection A Drug Inspector will visit your premises to verify documents and storage conditions. Get the License Issued Once approved, the license is granted digitally and can be downloaded from the portal. 📌 Key Conditions to Maintain Your License Appoint a qualified pharmacist or competent person full-time. Maintain cold storage or refrigeration for temperature-sensitive drugs. Display your license in a visible place at the premises. Renew the license before expiry to avoid penalties. Maintain proper records of purchase and sale of drugs. 📞 Need Assistance with Drug License in Haryana? Navigating drug license compliance can be time-consuming and confusing. Whether you’re setting up a new pharmacy, wholesale medicine shop, or expanding operations—PSR Compliance is here to help. Our experts handle everything from documentation and application to follow-up and inspection coordination. 👉 Apply confidently with professional help. Read the full article here: 🔗 https://www.psrcompliance.com/blog/drug-license-in-haryana
The High Stakes of FSSAI Compliance
At its core, a trademark is a recognizable sign, design, or expression that distinguishes products or services of a particular source from others. It can be a word, phrase, symbol, or even a combination of these. Think of the Nike swoosh or Apple’s iconic bitten apple—those are trademarks that carry powerful brand associations.
Starting a new company in Delhi is an exciting step—but it comes with important legal formalities. Whether you’re planning to launch a Private Limited Company, LLP, or Sole Proprietorship, registering your company correctly is the foundation of a compliant and successful business.
Planning to start a pharmacy, wholesale drug business, or medicine distribution unit in Delhi? You’ll need a valid drug license to operate legally. This guide covers the types of drug licenses, key requirements, application process, and why it's essential for your business. 👉 Read the full article here: https://www.psrcompliance.com/blog/introduction-to-drug-license-in-delhi
RNI registration is the process of getting official approval for the name and publication details of a periodical. It ensures that the publication name is unique and complies with legal norms. The registration is mandatory for all print media, including newspapers, weeklies, monthlies, and annual journals.
A trademark is like your business’s fingerprint—a unique sign that tells people your products or services come from you and not someone else. A trademark becomes your brand's identity in the marketplace, whether it’s a name, logo, slogan, or even a sound. Think of the golden arches of McDonald’s or the apple with a bite taken out of it—these aren’t just logos, they’re trademarks that represent billions in brand value.
