Key Rating Drivers & Detailed Description
Strengths:
Healthy business risk profile, supported by geographic diversity in revenue
The Emcure group has a diversified revenue profile, with 50% of revenue coming from the domestic market in fiscal 2022, 19% from emerging markets, 26% from regulated markets of Canada and Europe and the remaining from other segments, including contract manufacturing for Avet. The group has an established market position in the domestic formulations market with market share of 2.85% as per AIOCD MAT December 2022 and had nine brands in the top-300 brands in the domestic market. It also has a leading position in gynaecology, blood-related and human immunodeficiency virus (HIV) antiretroviral therapies.
Over the year, the group increased its presence in Europe and Canada by establishing frontend marketing networks through acquisitions of Tillomed Laboratories Ltd (UK) and Marcan Pharmaceuticals Inc (Canada). With demerger of Avet, the group’s consolidated revenue declined by 3% in fiscal 2022 (compared with 6-8% anticipated earlier); excluding the US business, the revenue grew by a healthy 16% year-on-year supported by strong growth in domestic and European markets. With new product launches and steady demand from existing markets, Emcure is expected to register revenue growth of 10-12% over the medium term.
Improved operating profitability with successful demerger of the US business
With demerger of the low-margin US business, consolidated operating margin improved to 23.3% in fiscal 2022 from 14-17% over fiscals 2018-2020. The improvement was also partly on account of better product mix, scaling up of high-margin domestic market leading to better absorption of costs and lower marketing and travelling cost amid the Covid-19 pandemic. With sustained high input cost and gradual increase in marketing spends, the operating margin is expected to moderate to 20-22% over the medium term, supported by focussed expansion in domestic markets and benefits of cost optimisation.
Experienced management team, accredited manufacturing facilities and established R&D capabilities
The promoter and CEO, Mr Satish Mehta, is a first-generation entrepreneur with almost four decades of experience in the pharma sector. The second generation has been actively involved in the strategy and growth initiatives of the business for over a decade. Additionally, the group has a team of highly qualified professionals and scientists to support operations, strategy and other functions, and drive future growth.
The group has 14 manufacturing facilities across India, which produce a range of pharma/ biopharma products in varied dosage forms, including oral solids, oral liquids, injectables, biologics, vaccines and complex APIs, such as chiral molecules and cytotoxic products. The facilities are approved/accredited by various regulatory bodies including, USFDA, MHRA (United Kingdom), Health Canada, EDQM (Europe), TGA Australia, ANVISA Brazil, HALMED Croatia, and are compliant with current Good Manufacturing Practices. The group does not have plans to undertake any major debt-funded capex.
It has five R&D facilities with over 500 scientists. Its R&D focus and manufacturing skills, developed through long track record of contract manufacturing for international pharma companies, has helped establish its presence in regulated and emerging markets. Besides, its generic formulations research in complex injectables, established expertise in chiral chemistry and focus on the biopharmaceutical business demonstrate its strong R&D capabilities.
Adequate financial risk profile
The financial risk profile remains adequate supported by sizeable networth. Albeit, debt protection metrics were moderate, as reflected in net adjusted debt to Ebitda ratio of 1.8 times in fiscal 2022. Interest coverage ratio was healthy at 8.1 times in fiscal 2022 owing to low cost of overseas borrowings. With debt levels expected to remain high because of higher utilisation of working capital limits and moderation in operating profitability, the net adjusted debt to Ebitda and interest coverage ratios are expected to moderate to ~1.9 times and ~6 times, respectively, in fiscal 2023. Aided by healthy cash accrual, moderate organic capex of Rs 300-350 crore annually and scheduled repayments, the key debt metrics are expected to improve in fiscal 2024; for instance, net adjusted debt to Ebitda ratio is expected to improve to less than 1.6 times in fiscal 2024. Steady improvement in debt metrics should continue over the medium term. While the group has some inorganic growth plans, any sizeable debt-funded acquisition could adversely impact debt metrics and liquidity and will remain a key monitorable.
The PE firm, Bain Capital, invested in the company in 2013 and holds13.09% stake. CRISIL Ratings understands that there is no obligation on Emcure or the promoter family to provide an exit or assured return to Bain Capital on its investment and Bain Capital will exit partly through the planned IPO.
Weaknesses:
Large working capital requirement
Operations are working capital intensive, as reflected in gross current assets of ~200 days as on March 31, 2022, driven by inventory and receivables of 118 and 83 days, respectively. The group operates in multiple geographies and has a large product portfolio; hence, it needs to maintain sizeable inventory to ensure adequate supply. It majorly has a tender-based business in emerging markets, wherein it extends credit of around 180 days, resulting in large receivables. Given the group’s continuously expanding geographical base and product portfolio, CRISIL Ratings believes the working capital requirement will remain large over the medium term.
Exposure to intensifying competition and increasing legal and regulatory risks
Emcure group generates significant proportion of total sales through the regulated markets. While the company has demerged its US business, sales to Europe and Canada will continue to form over 25% of total sales. The generics business in the regulated markets is highly competitive and has various legal and regulatory risks. Players in the regulated generics markets are vulnerable to pricing pressure on account of entry of several cost-competitive Indian players. Furthermore, with growing competition, the group will have to make investments in R&D and brands, which may limit improvement in profitability. Also, owing to the nature of products, the group, like many of its peers, is vulnerable to litigations filed by regulators among others. In addition, price-control measures of the government in the branded segment may weaken the growth in the domestic formulations market and remains a monitorable.
While the US business has been demerged, Emcure group remains exposed to the ongoing litigation in the US and other markets. Sizeable outflow towards settlement of the same remains a monitorable. Moreover, CRISIL Ratings notes that in March 2022, HDT Bio Corp, US-based biopharmaceutical company, filed a lawsuit against Emcure in a US court and an arbitration suit against Emcure’s subsidiary Gennova Biopharmaceuticals Ltd in the London Court of International Arbitration. In these suits, HDT has claimed that Emcure and Gennova misappropriated trade secrets related to Covid-19 vaccine development and has sought USD 950 million in damages. The management of Emcure and Gennova have maintained that there is no breach of contractual obligation or provisions of law. CRISIL Ratings will continue to monitor developments in this regard and will remain in discussion with the management of Emcure and Gennova to understand the likely implications, if any. Any adverse order or sizeable financial liability arising thereof would be a key monitorable.