Breaking Down Theravance Biopharma, Inc. (TBPH) Financial Health: Key Insights for Investors

Breaking Down Theravance Biopharma, Inc. (TBPH) Financial Health: Key Insights for Investors

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You're looking at Theravance Biopharma, Inc. (TBPH) right now and seeing a classic biotech inflection point: a solid commercial base meeting a high-stakes pipeline catalyst. The company just reported a strong Q3 2025, hitting non-GAAP breakeven, which is a defintely big deal for a development-stage company, plus they ended September 30 with a rock-solid balance sheet of $333 million in cash and zero debt. That cash gives them serious runway, but the real near-term opportunity is the $75 million in high-probability milestones expected in Q4 2025, split between YUPELRI and TRELEGY sales achievements. Still, the stock's movement is going to be dominated by the Phase 3 CYPRESS trial for ampreloxetine, with topline results due in Q1 2026; a positive readout could transform the company's valuation, but a setback carries a significant downside risk, so you need to understand exactly how the core business, which saw YUPELRI net sales jump 15% year-over-year to $71.4 million in Q3, acts as the financial cushion for that big R&D bet.

Revenue Analysis

The core takeaway for Theravance Biopharma, Inc. (TBPH) is a decisive shift in its revenue model, moving from a diversified royalty structure to one overwhelmingly focused on its collaboration with Viatris on YUPELRI, plus high-value near-term milestones. Total revenue for the first nine months of 2025 reached $61.57 million, representing a strong growth of approximately 34.9% compared to the same period in 2024.

Your revenue stream is now almost entirely derived from the Viatris collaboration revenue, which is a profit and loss sharing arrangement for the Chronic Obstructive Pulmonary Disease (COPD) treatment, YUPELRI (revefenacin). This collaboration revenue is TBPH's 35% share of YUPELRI's U.S. net sales, adjusted for shared commercial costs. For the third quarter of 2025, total revenue was $20.0 million, consisting entirely of this collaboration revenue, and it grew by 19% year-over-year (YoY).

The underlying product performance is solid. YUPELRI U.S. net sales, as recognized by Viatris, hit an all-time high of $71.4 million in Q3 2025, which was a 15% increase from Q3 2024. That's a significant jump, and it's defintely driven by strong customer demand and improved net pricing, especially in the crucial hospital channel where doses grew by 29% YoY in Q3 2025. This hospital momentum is the key growth engine for the near term.

Revenue Metric Q3 2025 Value YoY Growth (Q3 2025 vs. Q3 2024)
Total Revenue (TBPH Recognized) $20.0 million 19%
YUPELRI U.S. Net Sales (Viatris Recognized) $71.4 million 15%
Viatris Collaboration Revenue (TBPH Share) $20.0 million 19%

The most significant change in your revenue profile was the strategic monetization of the TRELEGY ELLIPTA royalty interest to GSK in Q2 2025, which brought in a one-time payment of $225 million. While future, long-term royalties are gone, you still have near-term, high-probability milestone payments (contingent payments) that act as powerful, non-recurring revenue injections. You are on track to trigger a $50 million milestone payment from Royalty Pharma in 2025 related to TRELEGY global net sales, and a $25 million milestone from Viatris for YUPELRI U.S. net sales hitting a $250 million threshold.

Here's the quick math on the near-term opportunities:

  • YUPELRI U.S. net sales need approximately $54 million in Q4 2025 to hit the $250 million annual target and trigger the $25 million milestone.
  • TRELEGY global net sales need about $471 million in Q4 2025 to trigger the $50 million milestone.
  • The TTM (Trailing Twelve Months) revenue sits at $80.33 million as of September 30, 2025, a 27.12% increase YoY, showing a clear upward trend in the core business.

This means your revenue is a mix of stable, growing collaboration revenue and large, lumpy milestone payments. To better understand the investor sentiment around these milestones, you should read Exploring Theravance Biopharma, Inc. (TBPH) Investor Profile: Who's Buying and Why?. Your action now is to monitor the Q4 2025 TRELEGY and YUPELRI sales data closely, as the achievement of these two milestones will add a combined $75 million to your 2025 fiscal year revenue.

Profitability Metrics

You need to know if Theravance Biopharma, Inc. (TBPH) is turning the corner from a development-stage burner of cash to a sustainable, profit-generating business. The short answer is yes, the shift is happening now, but you must look beyond the full-year trailing numbers to see it.

The company's profitability profile is a story of transition, moving from deep losses driven by research and development (R&D) to a recent, critical milestone: GAAP net income. Honestly, this is a major psychological and financial hurdle for any biotech firm.

Here's the quick math using the trailing twelve months (TTM) data ending June 2025, which gives us the most complete picture near the end of the fiscal year:

Metric (TTM to June 2025) Value (Millions USD) Margin
Revenue $77.21 N/A
Gross Profit $36.54 47.32%
Operating Income (Loss) ($35.63) -46.15%

What this estimate hides is the recent momentum. The TTM operating margin of -46.15% is a lagging indicator. The real news is the third quarter of 2025 (Q3 2025), where Theravance Biopharma, Inc. reported GAAP net income of $3.6 million on revenue of $19.99 million, translating to an 18.01% net profit margin for the quarter alone.

Operational Efficiency and Cost Management

The gross margin of 47.32% (TTM) is decent, but it's a far cry from the biotechnology industry average, which typically sits around 86.3% due to the high-margin nature of approved drugs. This gap reflects the company's revenue being a mix of their 35% share of YUPELRI net sales, which was $25.0 million in Q3 2025, plus other collaboration and royalty revenue, not just pure, unburdened drug sales.

The real story of operational efficiency is in the cost controls. Management has been defintely disciplined, achieving non-GAAP breakeven in Q3 2025. This is a direct result of tightly managing expenses while key product revenue grows.

  • R&D expense dropped to $8.1 million in Q3 2025.
  • Cost management drove non-GAAP operating income of $2.3 million in Q3 2025.
  • The company is on track to hit a $50 million milestone from Royalty Pharma in 2025 for TRELEGY sales.

Profitability Trend vs. Industry

The biotech industry overall is often characterized by negative profitability, with the average net profit margin sitting at a staggering -177.1% as companies spend heavily on R&D for future products. Theravance Biopharma, Inc.'s recent positive net income of $3.6 million in Q3 2025, reversing a net loss of $12.7 million in the same period last year, shows a clear and powerful trend toward financial maturity.

This recent swing to positive net income is a major de-risking event for investors. It means the core business is now generating enough profit to cover its costs, even as it continues to invest in its pipeline, like the pivotal Phase 3 CYPRESS study for ampreloxetine. For more on how the company plans to sustain this, review the Mission Statement, Vision, & Core Values of Theravance Biopharma, Inc. (TBPH).

Debt vs. Equity Structure

You're looking at Theravance Biopharma, Inc. (TBPH) and wondering how they fund their operations, especially in a capital-intensive sector like biotech. The direct takeaway is that Theravance Biopharma, Inc. operates with a remarkably conservative, debt-free capital structure, prioritizing non-dilutive funding from commercial assets over traditional debt financing.

As of the third quarter of the 2025 fiscal year, Theravance Biopharma, Inc. reported a balance sheet with no debt, meaning both long-term and short-term debt obligations were effectively zero. This is an unusual and powerful position for a biotechnology company, which often relies heavily on debt or constant equity raises to fund lengthy, expensive clinical trials. They had approximately $333 million in cash and equivalents at the end of Q3 2025, which gives them significant financial flexibility to advance their late-stage pipeline asset, ampreloxetine.

Here's the quick math on leverage: Since the company carries no traditional debt, their Debt-to-Equity (D/E) ratio is functionally zero. To be fair, a trailing twelve months (TTM) calculation that includes all liabilities shows a ratio of about 0.21, which is still incredibly low. This figure is substantially below the industry benchmark, indicating minimal financial risk from leverage.

  • Zero debt means no interest payments.
  • No interest payments frees up cash for R&D.
  • Low leverage reduces default risk significantly.

When you compare this to the Biotechnology industry's average Debt-to-Equity ratio, which is around 0.17 as of November 2025, Theravance Biopharma, Inc. is right in line with the most conservative, equity-focused peers, or even better, depending on the exact calculation. This capital discipline is a clear strategic choice, especially as they move toward a potential transformational data readout for ampreloxetine in early 2026.

The company's financing strategy strongly favors non-dilutive capital-money raised without issuing new shares or taking on debt. The most recent concrete example of this was the sale of their remaining royalty interest in TRELEGY ELLIPTA to GSK, which brought in a one-time, non-dilutive cash payment of $225 million in late Q2 2025. Plus, their profit-sharing arrangement for the commercialized drug YUPELRI provides a durable, growing revenue stream to fund operations, which further reduces the need for external financing. This focus on internal cash generation and royalty monetization over debt is what defines their capital structure. You can read more about their core business focus here: Mission Statement, Vision, & Core Values of Theravance Biopharma, Inc. (TBPH).

What this conservative structure hides is that they still need to manage their cash burn until a new drug is approved, but the low-risk approach is defintely a strength.

Financial Metric Theravance Biopharma, Inc. (TBPH) Value (FY 2025) Biotechnology Industry Average (Nov 2025)
Long-Term Debt $0 Varies
Short-Term Debt $0 Varies
Debt-to-Equity Ratio (TTM) 0.21 0.17
Major Q2/Q3 2025 Financing Activity $225 million royalty sale (non-debt) N/A

Your clear action is to monitor their cash runway and R&D spending against their milestone payments, as the debt-free balance sheet makes their cash position the most critical metric. Finance: track quarterly cash burn against the $333 million cash balance by the next earnings call.

Liquidity and Solvency

You want to know if Theravance Biopharma, Inc. (TBPH) has the cash to fund its operations and pipeline, and the short answer is a resounding yes. The company's liquidity position is defintely strong, primarily driven by a strategic asset sale in the second quarter of 2025, which has dramatically increased its cash reserves and working capital.

As of the end of the third quarter of 2025 (September 30, 2025), Theravance Biopharma, Inc. reported a robust balance sheet with $333 million in cash and no debt. This is a massive shift from the start of the year and provides a significant buffer to fund the pivotal Phase 3 CYPRESS study for ampreloxetine, which is a key near-term catalyst.

Current and Quick Ratios: A Liquidity Fortress

The company's ability to cover its short-term obligations (liquidity) is exceptional. The current ratio and quick ratio (acid-test ratio) are both in the double digits, which is a clear sign of financial strength. For a biotech company focused on late-stage development, this level of liquidity is a major risk mitigator.

Here's the quick math based on the Q3 2025 balance sheet data (in millions):

  • Current Assets: $354.7 million
  • Total Current Liabilities: $37.0 million
  • Quick Assets (excluding prepaid expenses): Approx. $347.9 million (Cash/Securities plus Receivables)
Liquidity Metric (Q3 2025) Calculation Value Interpretation
Current Ratio Current Assets / Current Liabilities 9.59:1 Exceptional; the company has $9.59 in current assets for every $1 in current liabilities.
Quick Ratio Quick Assets / Current Liabilities 9.40:1 Very strong; almost all current assets are highly liquid, indicating zero reliance on inventory.

A ratio of 1.0:1 is considered healthy, so a ratio over 9.0:1 means Theravance Biopharma, Inc. is sitting on a significant cash hoard relative to its short-term needs. This is the kind of financial firepower you want to see heading into a major clinical trial readout.

Working Capital Trends and Cash Flow Dynamics

Working capital (Current Assets minus Current Liabilities) has seen a dramatic increase, shifting from approximately $129.1 million at the end of 2024 to $317.7 million in Q3 2025. This massive jump is the key trend you need to understand, and it maps directly to a one-time financing event.

The cash flow statement overview for 2025 reveals a pivotal shift in the company's financial structure:

  • Operating Cash Flow (OCF) Trend: The company achieved non-GAAP breakeven in the third quarter of 2025, with non-GAAP net income from operations reaching $2.3 million. This marks a crucial transition toward self-funding operations, driven by durable revenue from their YUPELRI collaboration.
  • Investing and Financing Cash Flow: The most significant cash inflow was the completion of the strategic monetization of the TRELEGY royalty interest in Q2 2025, which brought in $225 million. This single transaction is the primary reason for the huge increase in the cash balance from $131 million in Q1 2025 to $339 million in Q2 2025.

The key takeaway is that the operating business is near-breakeven, which is good, but the current liquidity strength is due to a one-time financing move. This is a strategic trade-off: they sold a long-term royalty stream for immediate, high-value, non-dilutive cash to fund their current pipeline. You can read more about their corporate focus here: Mission Statement, Vision, & Core Values of Theravance Biopharma, Inc. (TBPH).

Potential Liquidity Strengths

The core strength is the $333 million cash balance and the absence of any long-term debt. This gives them a long runway, likely stretching well into 2027, even with ongoing R&D expenses projected between $32 million and $38 million for the full year 2025. Plus, they are on track to trigger a $50 million milestone payment from Royalty Pharma related to TRELEGY sales in 2025. This company has bought itself time and flexibility.

Valuation Analysis

You're looking at Theravance Biopharma, Inc. (TBPH) and asking the right question: is this stock priced correctly for the risk and opportunity? Based on the latest 2025 fiscal year data, the market is pricing in significant growth, which puts its valuation in a challenging spot, but the strong analyst consensus suggests a clear path to being undervalued.

As of mid-November 2025, the stock price sits around $18.03. This is an important number because the stock has been on a tear. Over the last 12 months, the price trend shows clear upward momentum, with the stock hitting a new 52-week high recently and the 50-day moving average of $14.23 sitting comfortably above the 200-day moving average of $12.14. That's a classic near-term bullish signal, but you have to look past the price chart and into the core ratios.

Here's the quick math on key valuation ratios for Theravance Biopharma, Inc. (TBPH) using 2025 data:

  • Price-to-Earnings (P/E) Ratio: The trailing twelve-month (TTM) P/E is high, around 31.09, but the forward P/E is notably lower at 23.99. This is the market telling you they expect earnings per share (EPS) to jump significantly in the next year. For a biopharma company, this is a growth valuation, not a value play.
  • Price-to-Book (P/B) Ratio: The P/B ratio is approximately 3.93. This is higher than the average for the broader pharmaceutical sector, suggesting investors are willing to pay nearly four times the company's net asset value for its pipeline and commercial assets like YUPELRI.
  • Enterprise Value-to-EBITDA (EV/EBITDA): This metric is less useful here because the company is still reporting negative EBITDA (Earnings Before Interest, Taxes, Depreciation, and Amortization), resulting in a negative EV/EBITDA of approximately -12.27. Instead, look at the EV-to-Sales ratio, which is around 7.79-a better gauge for a growth-focused, pre-profitability biotech.

The company does not pay a dividend, which is typical for a growth-stage biotech focused on reinvesting capital into its drug pipeline, so the dividend yield and payout ratios are both 0.00%. Don't expect passive income; expect capital appreciation tied to clinical success.

To be fair, the stock is currently trading below the Wall Street consensus. Analyst coverage is overwhelmingly positive, with a 'Strong Buy' or 'Buy' consensus rating from multiple firms. The average price target is about $24.25, which implies an upside of over 35% from the current price. This strong conviction from analysts, despite the high P/E, suggests they believe the company's clinical programs, especially ampreloxetine, and the durable cash flow from YUPELRI, which saw Q3 2025 net sales of $71.4 million, are undervalued by the current market price.

What this estimate hides is the binary risk of a clinical-stage asset. The high implied upside is directly tied to the success of their pipeline. If you want to dig deeper into who is buying and why, you can check out Exploring Theravance Biopharma, Inc. (TBPH) Investor Profile: Who's Buying and Why?

The bottom line: Theravance Biopharma, Inc. (TBPH) is not cheap on trailing earnings, but it is defintely undervalued if its pipeline delivers on the expected 2026 milestones. It's a high-conviction 'Buy' for growth investors, but a 'Hold' for anyone who can't stomach the volatility of a Phase 3 readout.

Risk Factors

You need to understand that Theravance Biopharma, Inc. (TBPH) is a biotech company, so its core risks are different from, say, a mature industrial firm. Simply put, your investment hinges on one major clinical event, and that creates a massive, near-term volatility window. The company's financial discipline is defintely a strength, but it doesn't eliminate the operational risk tied to its pipeline.

Operational and Strategic Risks: The Ampreloxetine Catalyst

The biggest internal risk is the binary outcome of ampreloxetine, their late-stage investigational drug for symptomatic neurogenic orthostatic hypotension (nOH) in Multiple System Atrophy (MSA) patients. The entire near-term valuation is tied to this single asset.

  • Clinical Trial Failure: Topline results from the pivotal Phase 3 CYPRESS study are expected in Q1 2026. A negative or inconclusive result would immediately and severely impact the stock price, as this is the primary growth driver.
  • Regulatory Hurdles: Even with positive Phase 3 data, there is always the risk of unfavorable decisions from the U.S. Food and Drug Administration (FDA) or other regulatory bodies on approval, labeling, or post-marketing requirements.
  • Commercialization Dependence: The company relies on key partners like Viatris for YUPELRI and GSK for TRELEGY Ellipta to handle commercialization, sales, and distribution. This dependence means Theravance Biopharma, Inc. (TBPH) has limited control over market execution and sales growth for its approved products.

Here's the quick math on their focus: They reaffirmed a full-year 2025 Research and Development (R&D) spend guidance of $32-$38 million, which is largely focused on advancing this pipeline, so the investment is concentrated.

Financial and External Risks in 2025

While Theravance Biopharma, Inc. (TBPH) has managed its balance sheet well, external market conditions and partnership agreements still pose clear financial risks. The company's financial health is currently robust, but its future cash flow is contingent on specific sales targets being met by third parties.

The company's dual-revenue stream from YUPELRI and TRELEGY Ellipta royalties provides crucial non-dilutive funding, but these revenues carry their own risks. For example, the achievement of a significant $50 million milestone payment from Royalty Pharma in 2025 is contingent on GSK's global net sales of TRELEGY Ellipta reaching approximately $3.41 billion for the fiscal year. If GSK's sales fall short, that cash injection disappears, which is a material hit to their expected 2025 revenue.

You should also factor in the competitive landscape for YUPELRI, their nebulized long-acting muscarinic antagonist (LAMA) for COPD. While Q3 2025 net sales were a record $71.4 million, up 15% year-over-year, continued growth is vulnerable to new or existing competitor therapies and pricing pressures in the respiratory market.

Risk Type 2025 Financial/Operational Impact Mitigation Strategy
Ampreloxetine Clinical Failure Potential loss of primary long-term value driver; stock price volatility. Disciplined capital deployment; strong cash balance of $333 million (Q3 2025) to fund operations without debt.
TRELEGY Milestone Miss Loss of a one-time $50 million cash payment if GSK's sales target is not met. Strategic monetization of a portion of TRELEGY royalties for a $225 million upfront payment in Q2 2025, de-risking long-term cash flow.
YUPELRI Competition Slower growth or decline in their 35% share of net sales, which was $25.0 million in Q3 2025. Focus on hospital channel adoption (a strong point in Q1 2025) and co-promotion efforts with Viatris.

Mitigation and Financial Stability

The good news is that management has taken clear steps to mitigate financial risk, which is what I look for. They achieved a non-GAAP breakeven in Q3 2025, which shows a focus on operational efficiency. Plus, the balance sheet is strong with no debt and a cash, cash equivalents, and marketable securities balance of $333 million as of September 30, 2025. That cash hoard gives them a significant runway to weather a clinical setback or market downturn without needing to raise dilutive capital immediately.

The strategic review committee, formed in late 2024, also signals a commitment to exploring all options to maximize shareholder value, which could mean further monetization of non-core assets or a strategic transaction. This is a smart move to keep options open. If you want a deeper dive into who is buying the stock right now, you should be Exploring Theravance Biopharma, Inc. (TBPH) Investor Profile: Who's Buying and Why?

Next step for you is simple: monitor the company's SEC filings for the Q4 2025 expense guidance and any updates on the ampreloxetine data readout timeline. Finance: track the TRELEGY sales data reported by GSK to gauge the likelihood of the $50 million milestone hitting the books.

Growth Opportunities

You're looking for where Theravance Biopharma, Inc. (TBPH) goes from here, and the answer is a clear pivot from a respiratory-focused model to a high-value rare disease play, all while maintaining a remarkably strong balance sheet. The company has essentially de-risked its near-term financing with its commercial assets, freeing up capital for the pipeline's big swing.

The core of their immediate growth is a dual-engine strategy: maximizing their commercial product, YUPELRI (revefenacin), and capitalizing on high-probability milestone payments. For the third quarter of 2025, YUPELRI U.S. net sales hit an all-time high of $71.4 million, a 15% year-over-year increase, driven by strong customer demand and improved pricing. TBPH's collaboration revenue, representing its 35% share of these net sales, was reported at approximately $19.99 million for Q3 2025. Honestly, that kind of steady, double-digit growth in a mature market like COPD is defintely a testament to their commercial partnership with Viatris.

The market expansion of YUPELRI into China is another clear tailwind. The early 2025 approval in this massive market triggered a $7.5 million milestone payment from Viatris. Plus, the company is set to achieve two near-term, high-probability financial catalysts in late 2025, totaling $75 million: a $50 million milestone from Royalty Pharma tied to TRELEGY sales and a $25 million milestone from Viatris for YUPELRI. That's significant non-dilutive capital.

Pipeline Innovation and Competitive Edge

The real value driver, and the source of their competitive edge, is ampreloxetine, a norepinephrine reuptake inhibitor (NRI) in Phase 3 development for symptomatic neurogenic orthostatic hypotension (nOH) in patients with Multiple System Atrophy (MSA). MSA is a rare, debilitating condition, and ampreloxetine has the potential to be a first-in-class precision therapy, which means a high-impact, high-margin market opportunity.

The pivotal Phase 3 CYPRESS study is the central focus. Enrollment completed in late summer 2025, and top-line results are expected in the first quarter of 2026. This is the single biggest catalyst for the stock in the next six months. If the data is positive, the market potential in this underserved rare disease space could be multi-hundred-million dollars.

Here is a quick overview of the 2025 financial position that supports this growth push:

Metric 2025 Fiscal Year Data Significance
Cash & Equivalents (as of 9/30/25) $333 million Strong liquidity; no debt.
Q3 2025 Collaboration Revenue $19.99 million Steady commercial base funding R&D.
Near-Term Milestones (Q4 2025) $75 million Immediate, high-probability cash injection.
Analyst FY 2025 Net Profit Projection Positive profits of $20 million Expected to achieve profitability in 2025.

Strategic Action and Near-Term Risk

The company is on track to achieve non-GAAP breakeven, demonstrating disciplined financial management, and analysts project they will generate positive profits of $20 million for the full year 2025. Their R&D expense guidance for the full year remains contained at $32 million to $38 million, which shows they are running an efficient, focused clinical program.

The competitive advantage here is a combination of financial strength and pipeline focus. They have $333 million in cash and no debt, which is rare for a biotech on the cusp of a Phase 3 readout. This financial discipline gives them strategic optionality (like the ongoing strategic review to unlock shareholder value) that many peers lack. The risk, to be fair, is all concentrated in the ampreloxetine trial data; a negative readout would necessitate a complete re-evaluation of the firm's long-term growth trajectory.

If you want a deeper dive into the numbers that support this outlook, you can read more here: Breaking Down Theravance Biopharma, Inc. (TBPH) Financial Health: Key Insights for Investors.

Your next step: Monitor the news flow around the December 2025 Key Opinion Leader (KOL) event on ampreloxetine, as it will be the final public commentary before the Q1 2026 data readout.

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